Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020179.2 | 1187 | Intron | NP_064564.1 | ||
XM_011542907.1 | 1187 | Intron | XP_011541209.1 | ||
XM_011542908.2 | 1187 | Intron | XP_011541210.1 | ||
XM_011542909.1 | 1187 | Intron | XP_011541211.1 | ||
XM_011542910.2 | 1187 | Missense Mutation | CAC,CGC | H141R | XP_011541212.1 |
XM_011542911.2 | 1187 | Missense Mutation | CAC,CGC | H115R | XP_011541213.1 |
XM_017018019.1 | 1187 | Missense Mutation | CAC,CGC | H136R | XP_016873508.1 |
XM_017018020.1 | 1187 | Intron | XP_016873509.1 |