Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152455.3 | 2956 | Missense Mutation | CAT,CGT | H790R | NP_689668.3 |
XM_006720401.3 | 2956 | Missense Mutation | CAT,CGT | H790R | XP_006720464.1 |
XM_011521266.2 | 2956 | Missense Mutation | CAT,CGT | H790R | XP_011519568.1 |
XM_017021949.1 | 2956 | Intron | XP_016877438.1 |