Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199818.1 | 777 | Intron | NP_001186747.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099410.1 | 777 | Missense Mutation | CCT,GCT | P18A | NP_001092880.1 |
NM_001099411.1 | 777 | Missense Mutation | CCT,GCT | P18A | NP_001092881.1 |
NM_001184727.1 | 777 | Missense Mutation | CCT,GCT | P18A | NP_001171656.1 |
NM_014710.4 | 777 | Missense Mutation | CCT,GCT | P18A | NP_055525.3 |
XM_017029981.1 | 777 | Missense Mutation | CCT,GCT | P18A | XP_016885470.1 |
XM_017029982.1 | 777 | Missense Mutation | CCT,GCT | P18A | XP_016885471.1 |