Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286350.1 | 784 | Intron | NP_001273279.1 | ||
NM_001286351.1 | 784 | Silent Mutation | CTA,CTG | L221L | NP_001273280.1 |
NM_214462.4 | 784 | Intron | NP_999627.2 | ||
XM_011535507.2 | 784 | Intron | XP_011533809.1 |