| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304562.1 | 588 | Intron | NP_001291491.1 | ||
| NM_001304563.1 | 588 | Missense Mutation | CGG,TGG | R168W | NP_001291492.1 |
| NM_173618.2 | 588 | Missense Mutation | CGG,TGG | R168W | NP_775889.1 |
| XM_011545809.2 | 588 | Missense Mutation | CGG,TGG | R168W | XP_011544111.1 |
| XM_011545811.2 | 588 | Missense Mutation | CGG,TGG | R168W | XP_011544113.1 |
| XM_011545812.2 | 588 | Missense Mutation | CGG,TGG | R168W | XP_011544114.1 |
| XM_017023169.1 | 588 | Missense Mutation | CGG,TGG | R168W | XP_016878658.1 |