Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024306.4 | 887 | Missense Mutation | ACG,ATG | T371M | NP_077282.3 |
XM_011523317.2 | 887 | Intron | XP_011521619.1 | ||
XM_011523319.2 | 887 | Missense Mutation | ACG,ATG | T291M | XP_011521621.1 |