| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015974.2 | 771 | Missense Mutation | CCT,TCT | P289S | NP_057058.2 |
| XM_005266415.3 | 771 | Missense Mutation | CCT,TCT | P235S | XP_005266472.1 |
| XM_005266416.4 | 771 | Intron | XP_005266473.1 | ||
| XM_017020624.1 | 771 | Missense Mutation | CCT,TCT | P204S | XP_016876113.1 |