| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024654.4 | 1105 | Missense Mutation | CCT,TCT | P695S | NP_078930.3 |
| XM_005263493.3 | 1105 | Missense Mutation | CCT,TCT | P408S | XP_005263550.1 |
| XM_011542147.2 | 1105 | Missense Mutation | CCT,TCT | P325S | XP_011540449.1 |
| XM_017002337.1 | 1105 | Intron | XP_016857826.1 | ||
| XM_017002338.1 | 1105 | Missense Mutation | CCT,TCT | P325S | XP_016857827.1 |
| XM_017002339.1 | 1105 | Missense Mutation | CCT,TCT | P325S | XP_016857828.1 |