Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001037.4 | 639 | Missense Mutation | CAC,CGC | H89R | NP_001028.1 |
NM_001321605.1 | 639 | Missense Mutation | CAC,CGC | H56R | NP_001308534.1 |
NM_199037.4 | 639 | Missense Mutation | CAC,CGC | H89R | NP_950238.1 |