Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152762.2 | 1352 | Missense Mutation | CAC,CGC | H374R | NP_689975.2 |
XM_011544887.2 | 1352 | Missense Mutation | CAC,CGC | H374R | XP_011543189.1 |
XM_011544888.2 | 1352 | Missense Mutation | CAC,CGC | H238R | XP_011543190.1 |