| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001257360.1 | 667 | Silent Mutation | CAA,CAG | Q78Q | NP_001244289.1 |
| NM_001257361.1 | 667 | Intron | NP_001244290.1 | ||
| NM_001308170.1 | 667 | Missense Mutation | AAG,AGG | K47R | NP_001295099.1 |
| NM_004037.7 | 667 | Silent Mutation | CAA,CAG | Q78Q | NP_004028.3 |
| NM_139156.3 | 667 | Intron | NP_631895.1 | ||
| NM_203404.1 | 667 | Intron | NP_981949.1 |