Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_080675.3 | 866 | Missense Mutation | CAC,CGC | H258R | NP_542406.2 |
XM_011528573.1 | 866 | Missense Mutation | CAC,CGC | H281R | XP_011526875.1 |
XM_011528574.1 | 866 | Missense Mutation | CAC,CGC | H233R | XP_011526876.1 |
XM_011528575.1 | 866 | Missense Mutation | CAC,CGC | H168R | XP_011526877.1 |
XM_011528576.1 | 866 | Intron | XP_011526878.1 |