Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006597.5 | 1652 | Missense Mutation | CTT,TTT | L459F | NP_006588.1 |
NM_153201.3 | 1652 | Missense Mutation | CTT,TTT | L459F | NP_694881.1 |
XM_011542798.1 | 1652 | Intron | XP_011541100.1 |