| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320952.1 | 1418 | Missense Mutation | CGG,TGG | R425W | NP_001307881.1 |
| NM_001320953.1 | 1418 | Missense Mutation | CGG,TGG | R407W | NP_001307882.1 |
| NM_001320954.1 | 1418 | Missense Mutation | CGG,TGG | R407W | NP_001307883.1 |
| NM_001320955.1 | 1418 | Missense Mutation | CGG,TGG | R406W | NP_001307884.1 |
| NM_014519.3 | 1418 | Missense Mutation | CGG,TGG | R434W | NP_055334.2 |
| XM_011524006.2 | 1418 | Missense Mutation | CGG,TGG | R386W | XP_011522308.1 |
| XM_017025021.1 | 1418 | Missense Mutation | CGG,TGG | R434W | XP_016880510.1 |
| XM_017025022.1 | 1418 | Missense Mutation | CGG,TGG | R358W | XP_016880511.1 |
| XM_017025023.1 | 1418 | Missense Mutation | CGG,TGG | R349W | XP_016880512.1 |