| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317948.1 | 727 | Intron | NP_001304877.1 | ||
| NM_173664.5 | 727 | Silent Mutation | CGG,TGG | R211W | NP_775935.1 |
| XM_011534529.2 | 727 | Intron | XP_011532831.1 | ||
| XM_011534530.2 | 727 | Intron | XP_011532832.1 | ||
| XM_011534531.2 | 727 | Intron | XP_011532833.1 | ||
| XM_017009372.1 | 727 | Intron | XP_016864861.1 |