Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001173514.1 | 149 | Intron | NP_001166985.1 | ||
NM_001173515.1 | 149 | Intron | NP_001166986.1 | ||
NM_003332.3 | 149 | Missense Mutation | CAT,CGT | H23R | NP_003323.1 |
NM_198125.2 | 149 | Missense Mutation | CAT,CGT | H23R | NP_937758.1 |