Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282291.1 | 435 | Missense Mutation | CAC,CGC | H131R | NP_001269220.1 |
NM_001282292.1 | 435 | Missense Mutation | CAC,CGC | H114R | NP_001269221.1 |
NM_001282293.1 | 435 | Intron | NP_001269222.1 | ||
NM_007188.4 | 435 | Missense Mutation | CAC,CGC | H114R | NP_009119.2 |