| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304550.1 | 1042 | Intron | NP_001291479.1 | ||
| NM_017736.4 | 1042 | Intron | NP_060206.2 | ||
| XM_011545891.1 | 1042 | Intron | XP_011544193.1 | ||
| XM_017023433.1 | 1042 | Missense Mutation | GCG,GTG | A292V | XP_016878922.1 |