Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286639.1 | 352 | Missense Mutation | ACG,ATG | T1M | NP_001273568.1 |
NM_001286640.1 | 352 | Intron | NP_001273569.1 | ||
NM_014940.3 | 352 | Missense Mutation | ACG,ATG | T1M | NP_055755.1 |