Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001024845.2 | 2182 | Silent Mutation | CTG,TTG | L586L | NP_001020016.1 |
NM_001261380.1 | 2182 | Silent Mutation | CTG,TTG | L590L | NP_001248309.1 |
NM_006934.3 | 2182 | Silent Mutation | CTG,TTG | L605L | NP_008865.2 |
NM_201649.3 | 2182 | Silent Mutation | CTG,TTG | L659L | NP_964012.2 |
XM_011542017.2 | 2182 | Intron | XP_011540319.1 | ||
XM_017002151.1 | 2182 | Silent Mutation | CTG,TTG | L586L | XP_016857640.1 |
XM_017002152.1 | 2182 | Silent Mutation | CTG,TTG | L559L | XP_016857641.1 |
XM_017002153.1 | 2182 | Silent Mutation | CTG,TTG | L548L | XP_016857642.1 |