Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024520.2 | 618 | Missense Mutation | CTC,TTC | L129F | NP_078796.2 |
XM_005246852.2 | 618 | Missense Mutation | CTC,TTC | L129F | XP_005246909.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039693.2 | 618 | Intron | NP_001034782.1 | ||
XM_017003310.1 | 618 | Intron | XP_016858799.1 |