| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000821.6 | 2161 | Missense Mutation | ACT,CCT | T747P | NP_000812.2 |
| NM_001142269.3 | 2161 | Missense Mutation | ACT,CCT | T690P | NP_001135741.1 |
| NM_001311312.1 | 2161 | Intron | NP_001298241.1 | ||
| XM_005264259.4 | 2161 | Missense Mutation | ACT,CCT | T745P | XP_005264316.1 |
| XM_011532764.2 | 2161 | Missense Mutation | ACT,CCT | T473P | XP_011531066.1 |
| XM_011532765.2 | 2161 | Missense Mutation | ACT,CCT | T473P | XP_011531067.1 |
| XM_017003803.1 | 2161 | Missense Mutation | ACT,CCT | T688P | XP_016859292.1 |