Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145829.1 | 369 | Missense Mutation | CAC,CGC | H116R | NP_001139301.1 |
NM_001145841.1 | 369 | Missense Mutation | CAC,CGC | H116R | NP_001139313.1 |
NM_003282.3 | 369 | Missense Mutation | CAC,CGC | H116R | NP_003273.1 |