| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166175.1 | 918 | UTR 3 | NP_001159647.1 | ||
| NM_001166176.1 | 918 | UTR 3 | NP_001159648.1 | ||
| NM_004387.3 | 918 | Missense Mutation | TCC,TTC | S145F | NP_004378.1 |
| XM_017009071.1 | 918 | Intron | XP_016864560.1 |