Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001280788.1 | 635 | Silent Mutation | CCC,CCT | P131P | NP_001267717.1 |
NM_001280789.1 | 635 | Silent Mutation | CCC,CCT | P146P | NP_001267718.1 |
NM_001280790.1 | 635 | Silent Mutation | CCC,CCT | P103P | NP_001267719.1 |
NM_001280791.1 | 635 | Silent Mutation | CCC,CCT | P103P | NP_001267720.1 |
NM_001280792.1 | 635 | Intron | NP_001267721.1 | ||
NM_001280793.1 | 635 | Silent Mutation | CCC,CCT | P29P | NP_001267722.1 |
NM_033161.3 | 635 | Silent Mutation | CCC,CCT | P146P | NP_149351.1 |
XM_011518943.1 | 635 | Silent Mutation | CCC,CCT | P137P | XP_011517245.1 |
XM_011518944.2 | 635 | Silent Mutation | CCC,CCT | P137P | XP_011517246.1 |
XM_011518945.2 | 635 | Intron | XP_011517247.1 | ||
XM_017015062.1 | 635 | Intron | XP_016870551.1 |