| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001254755.1 | 488 | Intron | NP_001241684.1 | ||
| NM_001254756.1 | 488 | Intron | NP_001241685.1 | ||
| NM_144611.3 | 488 | Missense Mutation | GAC,GGC | D69G | NP_653212.1 |
| XM_006721447.2 | 488 | Intron | XP_006721510.2 | ||
| XM_011523649.2 | 488 | Intron | XP_011521951.1 | ||
| XM_017024180.1 | 488 | Intron | XP_016879669.1 | ||
| XM_017024181.1 | 488 | Intron | XP_016879670.1 | ||
| XM_017024182.1 | 488 | Intron | XP_016879671.1 | ||
| XM_017024183.1 | 488 | Missense Mutation | GAC,GGC | D69G | XP_016879672.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015113.3 | 488 | Intron | NP_055928.3 | ||
| XM_005256561.2 | 488 | Intron | XP_005256618.1 | ||
| XM_011523759.2 | 488 | Intron | XP_011522061.1 | ||
| XM_017024382.1 | 488 | Intron | XP_016879871.1 | ||
| XM_017024383.1 | 488 | Intron | XP_016879872.1 | ||
| XM_017024384.1 | 488 | Intron | XP_016879873.1 |