| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286699.1 | 192 | UTR 5 | NP_001273628.1 | ||
| NM_001286700.1 | 192 | UTR 5 | NP_001273629.1 | ||
| NM_001286701.1 | 192 | Intron | NP_001273630.1 | ||
| NM_005772.4 | 192 | Missense Mutation | ACG,GCG | T2A | NP_005763.3 |
| XM_006716715.3 | 192 | UTR 5 | XP_006716778.1 | ||
| XM_011517673.2 | 192 | Intron | XP_011515975.1 | ||
| XM_017014176.1 | 192 | Intron | XP_016869665.1 |