Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302757.1 | 466 | Missense Mutation | ACT,GCT | T156A | NP_001289686.1 |
XM_011527251.2 | 466 | Missense Mutation | ACT,GCT | T82A | XP_011525553.1 |
XM_017027190.1 | 466 | Missense Mutation | ACT,GCT | T179A | XP_016882679.1 |
XM_017027191.1 | 466 | Missense Mutation | ACT,GCT | T155A | XP_016882680.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006233.4 | 466 | Intron | NP_006224.1 |