Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282489.2 | 1362 | Missense Mutation | CAC,CGC | H297R | NP_001269418.1 |
NM_173477.4 | 1362 | Missense Mutation | CAC,CGC | H400R | NP_775748.2 |
XM_011524296.2 | 1362 | Missense Mutation | CAC,CGC | H297R | XP_011522598.1 |