| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146039.1 | 89 | Missense Mutation | CCG,CGG | P21R | NP_001139511.1 |
| NM_001320252.1 | 89 | UTR 5 | NP_001307181.1 | ||
| NM_152281.2 | 89 | Missense Mutation | CCG,CGG | P21R | NP_689494.2 |
| XM_006711628.3 | 89 | UTR 5 | XP_006711691.1 | ||
| XM_011510149.2 | 89 | Missense Mutation | CCG,CGG | P21R | XP_011508451.1 |
| XM_011510150.2 | 89 | UTR 5 | XP_011508452.1 | ||
| XM_011510151.1 | 89 | UTR 5 | XP_011508453.1 | ||
| XM_017002807.1 | 89 | UTR 5 | XP_016858296.1 |