| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003712.3 | 676 | Missense Mutation | CGG,TGG | R193W | NP_003703.1 |
| NM_177526.2 | 676 | Missense Mutation | CGG,TGG | R137W | NP_803545.1 |
| NM_177543.2 | 676 | Missense Mutation | CGG,TGG | R214W | NP_808211.1 |
| XM_011528396.2 | 676 | Missense Mutation | CGG,TGG | R199W | XP_011526698.1 |