| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001160100.1 | 422 | Intron | NP_001153572.1 | ||
| NM_006984.4 | 422 | Intron | NP_008915.1 | ||
| NM_182848.3 | 422 | Missense Mutation | CCG,TCG | P63S | NP_878268.1 |
| XM_011521134.2 | 422 | Intron | XP_011519436.1 | ||
| XM_017020843.1 | 422 | Missense Mutation | CCG,TCG | P63S | XP_016876332.1 |
| XM_017020844.1 | 422 | Missense Mutation | CCG,TCG | P63S | XP_016876333.1 |