| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286828.1 | 137 | Missense Mutation | CCT,TCT | P26S | NP_001273757.1 |
| NM_198469.3 | 137 | Missense Mutation | CCT,TCT | P26S | NP_940871.2 |
| XM_005251877.4 | 137 | Missense Mutation | CCT,TCT | P26S | XP_005251934.1 |
| XM_005251878.3 | 137 | Missense Mutation | CCT,TCT | P15S | XP_005251935.1 |
| XM_006717034.3 | 137 | Missense Mutation | CCT,TCT | P26S | XP_006717097.1 |
| XM_011518457.2 | 137 | Missense Mutation | CCT,TCT | P26S | XP_011516759.1 |
| XM_011518458.1 | 137 | Missense Mutation | CCT,TCT | P11S | XP_011516760.1 |
| XM_017014578.1 | 137 | Intron | XP_016870067.1 |