| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001207047.2 | 377 | Intron | NP_001193976.1 | ||
| NM_001323332.1 | 377 | Missense Mutation | GCC,GTC | A96V | NP_001310261.1 |
| NM_139321.2 | 377 | Missense Mutation | GCC,GTC | A96V | NP_647537.1 |
| NM_139322.3 | 377 | Missense Mutation | GCC,GTC | A96V | NP_647538.1 |