Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003922.3 | 14366 | Silent Mutation | CCA,CCG | P4713P | NP_003913.3 |
XM_017022699.1 | 14366 | Silent Mutation | CCA,CCG | P4761P | XP_016878188.1 |
XM_017022700.1 | 14366 | Silent Mutation | CCA,CCG | P4749P | XP_016878189.1 |
XM_017022701.1 | 14366 | Silent Mutation | CCA,CCG | P4744P | XP_016878190.1 |
XM_017022702.1 | 14366 | Silent Mutation | CCA,CCG | P4744P | XP_016878191.1 |
XM_017022703.1 | 14366 | Silent Mutation | CCA,CCG | P4743P | XP_016878192.1 |
XM_017022704.1 | 14366 | Silent Mutation | CCA,CCG | P4737P | XP_016878193.1 |
XM_017022705.1 | 14366 | Silent Mutation | CCA,CCG | P4735P | XP_016878194.1 |
XM_017022706.1 | 14366 | Intron | XP_016878195.1 |