Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286775.1 | 206 | Intron | NP_001273704.1 | ||
NM_001286776.1 | 206 | Intron | NP_001273705.1 | ||
NM_138779.4 | 206 | Intron | NP_620134.3 | ||
XM_005254097.2 | 206 | Intron | XP_005254154.1 | ||
XM_011521135.2 | 206 | Intron | XP_011519437.1 | ||
XM_011521136.2 | 206 | Missense Mutation | CAT,CGT | H35R | XP_011519438.1 |
XM_017020852.1 | 206 | Intron | XP_016876341.1 |