| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001207071.1 | 372 | Intron | NP_001194000.1 | ||
| NM_001207072.1 | 372 | Intron | NP_001194001.1 | ||
| NM_001207073.1 | 372 | Intron | NP_001194002.1 | ||
| NM_001207074.1 | 372 | Intron | NP_001194003.1 | ||
| NM_138344.4 | 372 | Missense Mutation | GCC,GTC | A16V | NP_612353.3 |
| XM_011537297.1 | 372 | Intron | XP_011535599.1 |