Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130143.1 | 607 | Silent Mutation | GGC,GGG | G181G | NP_001123615.1 |
NM_017726.7 | 607 | Missense Mutation | CCT,GCT | P143A | NP_060196.1 |
XM_017022372.1 | 607 | UTR 3 | XP_016877861.1 |