Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282190.1 | 1675 | Missense Mutation | CAT,CGT | H342R | NP_001269119.1 |
NM_001282191.1 | 1675 | Intron | NP_001269120.1 | ||
NM_016478.4 | 1675 | Missense Mutation | CAT,CGT | H363R | NP_057562.3 |
XM_005250403.2 | 1675 | Missense Mutation | CAT,CGT | H239R | XP_005250460.1 |
XM_011516288.2 | 1675 | Missense Mutation | CAT,CGT | H296R | XP_011514590.1 |
XM_011516289.2 | 1675 | Missense Mutation | CAT,CGT | H273R | XP_011514591.1 |
XM_011516290.2 | 1675 | Missense Mutation | CAT,CGT | H195R | XP_011514592.1 |
XM_017012287.1 | 1675 | Missense Mutation | CAT,CGT | H320R | XP_016867776.1 |
XM_017012288.1 | 1675 | Missense Mutation | CAT,CGT | H195R | XP_016867777.1 |