Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318326.1 | 339 | Missense Mutation | CTT,TTT | L36F | NP_001305255.1 |
NM_001318327.1 | 339 | Intron | NP_001305256.1 | ||
NM_015221.3 | 339 | Intron | NP_056036.1 | ||
XM_006717735.2 | 339 | Intron | XP_006717798.1 | ||
XM_011539559.2 | 339 | Intron | XP_011537861.1 |