Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077261.3 | 7487 | Intron | NP_001070729.2 | ||
NM_001206654.1 | 7487 | Missense Mutation | CAC,CGC | H2379R | NP_001193583.1 |
NM_006312.5 | 7487 | Missense Mutation | CAC,CGC | H2389R | NP_006303.4 |