Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001326380.1 | 567 | Silent Mutation | CCG,CCT | P110P | NP_001313309.1 |
NM_001326381.1 | 567 | Silent Mutation | CCG,CCT | P99P | NP_001313310.1 |
NM_014320.2 | 567 | Silent Mutation | CCG,CCT | P99P | NP_055135.1 |
XM_017010631.1 | 567 | Silent Mutation | CCG,CCT | P99P | XP_016866120.1 |