| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286633.1 | 986 | Missense Mutation | CGG,TGG | R57W | NP_001273562.1 |
| NM_138700.4 | 986 | Missense Mutation | CGG,TGG | R57W | NP_619645.1 |
| XM_011514305.1 | 986 | Missense Mutation | CGG,TGG | R57W | XP_011512607.1 |
| XM_011514306.1 | 986 | Missense Mutation | CGG,TGG | R57W | XP_011512608.1 |
| XM_011514308.1 | 986 | Missense Mutation | CGG,TGG | R57W | XP_011512610.1 |
| XM_011514309.1 | 986 | Missense Mutation | CGG,TGG | R57W | XP_011512611.1 |