Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130143.1 | 419 | Missense Mutation | CCC,CGC | P128R | NP_001123615.1 |
NM_017726.7 | 419 | Silent Mutation | ACC,ACG | T89T | NP_060196.1 |
XM_017022372.1 | 419 | Silent Mutation | ACC,ACG | T89T | XP_016877861.1 |