Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001104544.1 | 572 | Intron | NP_001098014.1 | ||
NM_001104545.1 | 572 | Intron | NP_001098015.1 | ||
NM_017938.3 | 572 | Intron | NP_060408.3 | ||
XM_017029619.1 | 572 | Intron | XP_016885108.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001184742.1 | 572 | Missense Mutation | CCC,CTC | P82L | NP_001171671.1 |
NM_006777.3 | 572 | Missense Mutation | CCC,CTC | P82L | NP_006768.1 |