Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080450.2 | 2887 | Missense Mutation | CAC,CGC | H746R | NP_001073919.1 |
XM_005267079.3 | 2887 | Intron | XP_005267136.1 | ||
XM_005267080.3 | 2887 | Missense Mutation | CAC,CGC | H746R | XP_005267137.1 |
XM_011536005.2 | 2887 | Intron | XP_011534307.1 | ||
XM_017011138.1 | 2887 | Missense Mutation | CAC,CGC | H746R | XP_016866627.1 |