| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024807.2 | 616 | Missense Mutation | CCT,TCT | P142S | NP_001019978.1 |
| NM_005166.4 | 616 | Missense Mutation | CCT,TCT | P142S | NP_005157.1 |
| XM_017026737.1 | 616 | Missense Mutation | CCT,TCT | P142S | XP_016882226.1 |
| XM_017026738.1 | 616 | Missense Mutation | CCT,TCT | P142S | XP_016882227.1 |