| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144.5 | 1733 | Missense Mutation | CGG,TGG | R635W | NP_001135.3 |
| NM_001323511.1 | 1733 | Missense Mutation | CGG,TGG | R540W | NP_001310440.1 |
| NM_001323512.1 | 1733 | Missense Mutation | CGG,TGG | R667W | NP_001310441.1 |
| XM_005255890.3 | 1733 | Missense Mutation | CGG,TGG | R540W | XP_005255947.1 |