| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135721.1 | 397 | Missense Mutation | CGG,TGG | R90W | NP_001129193.1 |
| NM_018068.3 | 397 | Missense Mutation | CGG,TGG | R90W | NP_060538.2 |
| XM_005273550.4 | 397 | Missense Mutation | CGG,TGG | R90W | XP_005273607.1 |
| XM_005273551.3 | 397 | Missense Mutation | CGG,TGG | R90W | XP_005273608.1 |