| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286521.1 | 996 | Missense Mutation | TGC,TGG | C235W | NP_001273450.1 |
| NM_001286522.1 | 996 | Missense Mutation | TGC,TGG | C235W | NP_001273451.1 |
| NM_020367.5 | 996 | Missense Mutation | TGC,TGG | C316W | NP_065100.2 |
| XM_005253711.4 | 996 | Missense Mutation | TGC,TGG | C309W | XP_005253768.1 |
| XM_011520970.1 | 996 | Missense Mutation | TGC,TGG | C309W | XP_011519272.1 |
| XM_011520971.2 | 996 | Missense Mutation | TGC,TGG | C309W | XP_011519273.1 |
| XM_011520973.2 | 996 | Missense Mutation | TGC,TGG | C309W | XP_011519275.1 |
| XM_017019670.1 | 996 | Missense Mutation | TGC,TGG | C309W | XP_016875159.1 |
| XM_017019671.1 | 996 | Missense Mutation | TGC,TGG | C235W | XP_016875160.1 |