| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001100620.1 | 673 | Intron | NP_001094090.1 | ||
| NM_001278324.1 | 673 | Intron | NP_001265253.1 | ||
| NM_005480.3 | 673 | Missense Mutation | GCC,GTC | A169V | NP_005471.3 |
| XM_006719181.1 | 673 | Missense Mutation | GCC,GTC | A169V | XP_006719244.1 |
| XM_011537723.1 | 673 | Missense Mutation | GCC,GTC | A169V | XP_011536025.1 |
| XM_011537724.1 | 673 | UTR 5 | XP_011536026.1 | ||
| XM_011537725.2 | 673 | Intron | XP_011536027.1 |