| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001662.1 | 1908 | Missense Mutation | CCT,TCT | P477S | NP_001001662.1 |
| XM_005251742.4 | 1908 | Missense Mutation | CCT,TCT | P477S | XP_005251799.1 |
| XM_005251744.3 | 1908 | Missense Mutation | CCT,TCT | P453S | XP_005251801.1 |
| XM_011518315.2 | 1908 | Missense Mutation | CCT,TCT | P477S | XP_011516617.1 |
| XM_011518318.2 | 1908 | Missense Mutation | CCT,TCT | P477S | XP_011516620.1 |
| XM_011518320.2 | 1908 | Missense Mutation | CCT,TCT | P471S | XP_011516622.1 |
| XM_017014343.1 | 1908 | Missense Mutation | CCT,TCT | P471S | XP_016869832.1 |
| XM_017014344.1 | 1908 | Missense Mutation | CCT,TCT | P345S | XP_016869833.1 |