| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199216.1 | 314 | Missense Mutation | TCC,TTC | S14F | NP_001186145.1 |
| NM_002361.3 | 314 | Missense Mutation | TCC,TTC | S39F | NP_002352.1 |
| NM_080600.2 | 314 | Missense Mutation | TCC,TTC | S39F | NP_542167.1 |