| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001110533.1 | 352 | Missense Mutation | CGG,TGG | R100W | NP_001104003.1 |
| NM_152607.2 | 352 | Missense Mutation | CGG,TGG | R100W | NP_689820.2 |
| XM_017000480.1 | 352 | Missense Mutation | CGG,TGG | R100W | XP_016855969.1 |
| XM_017000481.1 | 352 | Missense Mutation | CGG,TGG | R100W | XP_016855970.1 |