| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001167606.1 | 529 | Silent Mutation | GGC,GGT | G146G | NP_001161078.1 |
| NM_006861.6 | 529 | Missense Mutation | GCG,GTG | A188V | NP_006852.1 |
| XM_011537779.1 | 529 | UTR 5 | XP_011536081.1 | ||
| XM_017018723.1 | 529 | UTR 5 | XP_016874212.1 |