| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098520.1 | 362 | Missense Mutation | GCT,GGT | A133G | NP_001091990.1 |
| NM_001098521.1 | 362 | Missense Mutation | GCT,GGT | A99G | NP_001091991.1 |
| NM_001098522.1 | 362 | Missense Mutation | GCT,GGT | A99G | NP_001091992.1 |
| NM_001098523.1 | 362 | Missense Mutation | GCT,GGT | A99G | NP_001091993.1 |
| NM_006410.4 | 362 | Missense Mutation | GCT,GGT | A99G | NP_006401.3 |