Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282933.1 | 297 | Missense Mutation | ACG,ATG | T12M | NP_001269862.1 |
NM_001282935.1 | 297 | UTR 5 | NP_001269864.1 | ||
NM_032819.4 | 297 | Missense Mutation | ACG,ATG | T12M | NP_116208.3 |