| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001258288.1 | 1414 | Missense Mutation | TCC,TGC | S309C | NP_001245217.1 |
| NM_001258289.1 | 1414 | Missense Mutation | TCC,TGC | S413C | NP_001245218.1 |
| NM_003944.3 | 1414 | Missense Mutation | TCC,TGC | S371C | NP_003935.2 |
| XM_017002757.1 | 1414 | Intron | XP_016858246.1 |