| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317936.1 | 731 | Missense Mutation | AGT,CGT | S29R | NP_001304865.1 |
| NM_213605.2 | 731 | Missense Mutation | AGT,CGT | S29R | NP_998770.2 |
| XM_011517014.2 | 731 | Missense Mutation | AGT,CGT | S29R | XP_011515316.1 |
| XM_011517015.2 | 731 | Missense Mutation | AGT,CGT | S29R | XP_011515317.1 |
| XM_011517017.2 | 731 | Intron | XP_011515319.1 | ||
| XM_017013384.1 | 731 | Intron | XP_016868873.1 |