Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039132.2 | 555 | Silent Mutation | GCA,GCG | A144A | NP_001034221.1 |
NM_001544.4 | 555 | Missense Mutation | CAT,CGT | H170R | NP_001535.1 |
NM_022377.3 | 555 | Missense Mutation | CAT,CGT | H170R | NP_071772.1 |