Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_080605.3 | 707 | Missense Mutation | CAC,CGC | H226R | NP_542172.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016176.3 | 707 | Intron | NP_057260.2 | ||
NM_016547.2 | 707 | Intron | NP_057631.1 | ||
XM_011541556.1 | 707 | Intron | XP_011539858.1 |