| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001079911.2 | 1058 | Missense Mutation | CCT,TCT | P27S | NP_001073380.1 |
| NM_004407.3 | 1058 | Missense Mutation | CCT,TCT | P27S | NP_004398.1 |
| XM_011531705.2 | 1058 | Missense Mutation | CCT,TCT | P56S | XP_011530007.1 |
| XM_011531706.2 | 1058 | Missense Mutation | CCT,TCT | P56S | XP_011530008.1 |