Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039132.2 | 977 | Missense Mutation | ACG,ATG | T236M | NP_001034221.1 |
NM_001544.4 | 977 | Missense Mutation | CGC,TGC | R262C | NP_001535.1 |
NM_022377.3 | 977 | UTR 3 | NP_071772.1 |