| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040152.1 | 392 | UTR 5 | NP_001035242.1 | ||
| NM_001172437.2 | 392 | Missense Mutation | TGC,TGG | C47W | NP_001165908.1 |
| NM_001172438.2 | 392 | Missense Mutation | TGC,TGG | C47W | NP_001165909.1 |
| NM_001184961.1 | 392 | Missense Mutation | TGC,TGG | C5W | NP_001171890.1 |
| NM_001184962.1 | 392 | Missense Mutation | TGC,TGG | C5W | NP_001171891.1 |
| NM_015068.3 | 392 | UTR 5 | NP_055883.2 |