| 1041 | TRINITY_DN3289_c0_g1_i2 | Ll_transcript_347531 | complete | - | - | - | - | - | - | - | - | XP_019430116.1 | - | - | |
| 1042 | TRINITY_DN32905_c0_g1_i1 | Ll_transcript_530837 | 5prime_partial | - | S-formylglutathione hydrolase from Homo with 54.78% of identity | - | - | - | - | - | - | XP_003519088.1 | - | - | |
| 1043 | TRINITY_DN32922_c0_g1_i1 | Ll_transcript_530825 | complete | - | - | - | - | - | - | - | - | XP_014631533.1 | - | - | |
| 1044 | TRINITY_DN32932_c0_g1_i1 | Ll_transcript_530831 | 5prime_partial | - | - | - | - | - | - | - | - | XP_013461253.1 | - | - | |
| 1045 | TRINITY_DN32943_c0_g1_i1 | Ll_transcript_530832 | internal | Mechanosensitive ion channel protein 8 from Arabidopsis with 56.72% of identity | Mechanosensitive ion channel protein 8 from Arabidopsis with 56.72% of identity | - | - | - | - | AT2G17010 (ath) | CNT0000406 | XP_019438255.1 | GO:0012505 | - | |
| 1046 | TRINITY_DN32959_c0_g1_i1 | Ll_transcript_530819 | internal | L-ascorbate oxidase homolog from Brassica with 47.09% of identity | L-ascorbate oxidase homolog from Brassica with 47.09% of identity | Multicopper oxidase (PF00394.21) | - | - | - | 106452325 (bna) | - | XP_019433262.1 | GO:0005576 | GO:0055114 | |
| 1047 | TRINITY_DN3297_c0_g1_i1 | Ll_transcript_347553 | complete | - | - | - | - | - | - | - | - | NP_001236104.2 | - | - | |
| 1048 | TRINITY_DN33008_c0_g1_i1 | Ll_transcript_325305 | internal | Disease resistance protein TAO1 from Arabidopsis with 38.94% of identity | Disease resistance protein TAO1 from Arabidopsis with 38.94% of identity | TIR domain (PF01582.19) | - | leucine Rich Repeat(COG4886) | - | AT5G44510 (ath) | - | XP_019433712.1 | GO:0043531 | GO:0005515 | |
| 1049 | TRINITY_DN33064_c0_g1_i1 | Ll_transcript_325298 | 5prime_partial | Transcription factor RADIALIS from Antirrhinum with 58.97% of identity | Transcription factor RADIALIS from Antirrhinum with 58.97% of identity | - | - | - | - | - | - | XP_006573585.1 | GO:0005634 | - | |
| 1050 | TRINITY_DN33069_c0_g2_i1 | Ll_transcript_325288 | 5prime_partial | 60S ribosomal protein L22 from Sophophora with 70.73% of identity | 60S ribosomal protein L22 from Silurana with 76.53% of identity | Ribosomal L22e protein family (PF01776.16) | - | Ribosomal protein(ENOG4111UVJ) | - | Dmel_CG7434 (dme) | - | XP_016205560.1 | GO:0022625 | GO:0003735 | |
| 1051 | TRINITY_DN3307_c0_g1_i1 | Ll_transcript_477474 | internal | - | - | - | - | - | - | - | - | XP_003621226.1 | - | - | |
| 1052 | TRINITY_DN3307_c0_g1_i2 | Ll_transcript_477475 | internal | - | - | - | - | - | - | - | - | XP_003621226.1 | - | - | |
| 1053 | TRINITY_DN3309_c0_g1_i1 | Ll_transcript_477485 | 3prime_partial | 40S ribosomal protein S20 from Xenopus with 79.49% of identity | 40S ribosomal protein S20 from Xenopus with 79.49% of identity | Ribosomal protein S10p/S20e (PF00338.21) | - | - | - | 379094 (xla) | - | XP_019431524.1 | GO:0015935 | - | |
| 1054 | TRINITY_DN330_c0_g1_i1 | Ll_transcript_428308 | 3prime_partial | Probable rRNA-processing protein ebp2 from Schizosaccharomyces with 45.13% of identity | Probable rRNA-processing protein ebp2 from Schizosaccharomyces with 45.13% of identity | Eukaryotic rRNA processing protein EBP2 (PF05890.11) | - | - | - | SPAC17H9.05 (spo) | - | XP_003612737.2 | GO:0044732 | - | |
| 1055 | TRINITY_DN33144_c0_g1_i1 | Ll_transcript_277580 | 5prime_partial | Probable N-acetyltransferase HLS1-like from Arabidopsis with 72.66% of identity | Probable N-acetyltransferase HLS1-like from Arabidopsis with 72.66% of identity | - | - | Acetyltransferase (GNAT) family(ENOG410YF8W) | - | AT2G23060 (ath) | - | XP_019444962.1 | GO:0008080 | - | |
| 1056 | TRINITY_DN33151_c0_g1_i1 | Ll_transcript_277579 | internal | - | UNC93-like protein C922.05c from Schizosaccharomyces with 47.3% of identity | - | - | - | - | SPAC922.05c (spo) | - | XP_017420601.1 | GO:0005737 | - | |
| 1057 | TRINITY_DN33204_c0_g1_i1 | Ll_transcript_470585 | complete | NDR1/HIN1-like protein 2 from Arabidopsis with 44.59% of identity | NDR1/HIN1-like protein 3 from Arabidopsis with 48.07% of identity | Late embryogenesis abundant protein (PF03168.12) | - | harpin-induced protein 1 domain containing protein, expressed(ENOG410YGQV) | - | AT3G11650 (ath) | - | XP_019433866.1 | GO:0046658 | - | |
| 1058 | TRINITY_DN33226_c0_g1_i1 | Ll_transcript_470582 | complete | Protein SPEAR1 from Arabidopsis with 44.33% of identity | Protein SPEAR3 from Arabidopsis with 44% of identity | - | - | NA(ENOG410Z28R) | - | AT2G20080 (ath) | - | XP_019447703.1 | GO:0006355 | - | |
| 1059 | TRINITY_DN33245_c0_g2_i1 | Ll_transcript_470581 | complete | - | - | - | - | - | - | - | - | XP_004491334.1 | - | - | |
| 1060 | TRINITY_DN3327_c0_g1_i1 | Ll_transcript_477482 | complete | Histone H4 from Soja with 100% of identity | Histone H4 from Soja with 100% of identity | Centromere kinetochore component CENP-T histone fold (PF15511.5) | - | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling(COG2036) | - | 100305586 (gmx) | - | XP_007162656.1 | GO:0000788 | GO:0006352 | |