| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001127229.1 | 580 | Missense Mutation | CGG,TGG | R136W | NP_001120701.1 |
| NM_001127230.1 | 580 | Missense Mutation | CGG,TGG | R136W | NP_001120702.1 |
| NM_017900.2 | 580 | Missense Mutation | CGG,TGG | R136W | NP_060370.1 |
| XM_011541670.2 | 580 | Missense Mutation | CGG,TGG | R165W | XP_011539972.1 |