Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005865.3 | 423 | Silent Mutation | CTG,CTT | L136L | NP_005856.1 |
XM_017010161.1 | 423 | Silent Mutation | CTG,CTT | L136L | XP_016865650.1 |
XM_017010162.1 | 423 | Silent Mutation | CTG,CTT | L136L | XP_016865651.1 |
XM_017010163.1 | 423 | Silent Mutation | CTG,CTT | L136L | XP_016865652.1 |
XM_017010164.1 | 423 | Silent Mutation | CTG,CTT | L136L | XP_016865653.1 |
XM_017010165.1 | 423 | Intron | XP_016865654.1 |