| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271440.1 | 1173 | Intron | NP_001258369.1 | ||
| NM_001271441.1 | 1173 | Missense Mutation | GCG,GTG | A322V | NP_001258370.1 |
| NM_001271442.1 | 1173 | Intron | NP_001258371.1 | ||
| NM_004928.2 | 1173 | Intron | NP_004919.1 | ||
| XM_006724051.3 | 1173 | Intron | XP_006724114.1 | ||
| XM_006724053.3 | 1173 | Intron | XP_006724116.1 | ||
| XM_017028470.1 | 1173 | Intron | XP_016883959.1 | ||
| XM_017028471.1 | 1173 | Intron | XP_016883960.1 | ||
| XM_017028472.1 | 1173 | Intron | XP_016883961.1 |