| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159587.2 | 357 | Missense Mutation | CGG,TGG | R27W | NP_001153059.1 |
| NM_001159588.2 | 357 | Missense Mutation | CGG,TGG | R27W | NP_001153060.1 |
| NM_133493.4 | 357 | Missense Mutation | CGG,TGG | R27W | NP_598000.2 |
| XM_005248659.3 | 357 | Missense Mutation | CGG,TGG | R27W | XP_005248716.1 |
| XM_011535473.1 | 357 | Missense Mutation | CGG,TGG | R14W | XP_011533775.1 |
| XM_017010283.1 | 357 | Intron | XP_016865772.1 |