| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000079.3 | 1333 | Missense Mutation | AGG,TGG | R419W | NP_000070.1 |
| NM_001039523.2 | 1333 | Missense Mutation | AGG,TGG | R444W | NP_001034612.1 |
| XM_017003256.1 | 1333 | Missense Mutation | AGG,TGG | R451W | XP_016858745.1 |
| XM_017003257.1 | 1333 | Missense Mutation | AGG,TGG | R426W | XP_016858746.1 |