Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171905.1 | 170 | Missense Mutation | CAC,CGC | H32R | NP_001165376.1 |
NM_001171906.1 | 170 | Missense Mutation | CAC,CGC | H78R | NP_001165377.1 |
NM_152395.2 | 170 | Missense Mutation | CAC,CGC | H78R | NP_689608.2 |