| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001293291.1 | 527 | Missense Mutation | CGG,TGG | R77W | NP_001280220.1 |
| NM_001293294.1 | 527 | Missense Mutation | CGG,TGG | R19W | NP_001280223.1 |
| NM_001293296.1 | 527 | Missense Mutation | CGG,TGG | R19W | NP_001280225.1 |
| NM_001300923.1 | 527 | Missense Mutation | CGG,TGG | R19W | NP_001287852.1 |
| NM_001300924.1 | 527 | Missense Mutation | CGG,TGG | R19W | NP_001287853.1 |
| NM_138768.3 | 527 | Missense Mutation | CGG,TGG | R77W | NP_620123.2 |