Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001060.5 | 1352 | Missense Mutation | CAC,CGC | H322R | NP_001051.1 |
NM_201636.2 | 1352 | Missense Mutation | CAC,CGC | H322R | NP_963998.2 |
XM_011528214.2 | 1352 | Missense Mutation | CAC,CGC | H322R | XP_011526516.1 |