Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005419.3 | 1660 | Silent Mutation | CCA,CCG | P709P | NP_005410.1 |
NM_198332.1 | 1660 | Silent Mutation | CCA,CCG | P705P | NP_938146.1 |
XM_005269111.3 | 1660 | Intron | XP_005269168.2 | ||
XM_011538697.2 | 1660 | Silent Mutation | CCA,CCG | P717P | XP_011536999.1 |
XM_011538698.2 | 1660 | Silent Mutation | CCA,CCG | P713P | XP_011537000.1 |
XM_011538699.2 | 1660 | Intron | XP_011537001.1 | ||
XM_011538700.2 | 1660 | Silent Mutation | CCA,CCG | P473P | XP_011537002.1 |
XM_017019904.1 | 1660 | Silent Mutation | CCA,CCG | P465P | XP_016875393.1 |