Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318916.1 | 762 | Intron | NP_001305845.1 | ||
NM_018453.3 | 762 | Intron | NP_060923.2 | ||
XM_011536958.1 | 762 | Intron | XP_011535260.1 | ||
XM_017021460.1 | 762 | Missense Mutation | TGT,TTT | C218F | XP_016876949.1 |