Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001269053.1 | 172 | Silent Mutation | CCA,CCG | P29P | NP_001255982.1 |
NM_138812.3 | 172 | Silent Mutation | CCA,CCG | P29P | NP_620167.1 |
XM_005269549.4 | 172 | Silent Mutation | CCA,CCG | P29P | XP_005269606.1 |
XM_005269550.4 | 172 | Silent Mutation | CCA,CCG | P29P | XP_005269607.1 |
XM_011539334.2 | 172 | Silent Mutation | CCA,CCG | P29P | XP_011537636.1 |
XM_011539335.1 | 172 | Silent Mutation | CCA,CCG | P29P | XP_011537637.1 |
XM_017015749.1 | 172 | Silent Mutation | CCA,CCG | P29P | XP_016871238.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001270041.1 | 172 | Intron | NP_001256970.1 | ||
NM_001270042.1 | 172 | Intron | NP_001256971.1 | ||
NM_032372.5 | 172 | Intron | NP_115748.1 | ||
XM_011540267.2 | 172 | Intron | XP_011538569.1 | ||
XM_011540268.1 | 172 | Intron | XP_011538570.1 | ||
XM_011540270.2 | 172 | Intron | XP_011538572.1 |