| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010909.3 | 1698 | Missense Mutation | AGT,GGT | S461G | NP_001010909.2 |
| NM_001322370.1 | 1698 | Missense Mutation | NP_001309299.1 | ||
| NM_001322371.1 | 1698 | Missense Mutation | NP_001309300.1 |