| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130045.1 | 442 | Silent Mutation | GCG,GCT | A44A | NP_001123517.1 |
| NM_153254.2 | 442 | Intron | NP_694986.2 | ||
| XM_005244738.1 | 442 | UTR 5 | XP_005244795.1 | ||
| XM_011541177.2 | 442 | Silent Mutation | GCG,GCT | A44A | XP_011539479.1 |
| XM_017000906.1 | 442 | Intron | XP_016856395.1 | ||
| XM_017000907.1 | 442 | Silent Mutation | GCG,GCT | A44A | XP_016856396.1 |
| XM_017000908.1 | 442 | Silent Mutation | GCG,GCT | A44A | XP_016856397.1 |
| XM_017000909.1 | 442 | Silent Mutation | GCG,GCT | A44A | XP_016856398.1 |
| XM_017000910.1 | 442 | Silent Mutation | GCG,GCT | A44A | XP_016856399.1 |
| XM_017000911.1 | 442 | Silent Mutation | GCG,GCT | A44A | XP_016856400.1 |
| XM_017000912.1 | 442 | Silent Mutation | GCG,GCT | A44A | XP_016856401.1 |