Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001323614.1 | 296 | Intron | NP_001310543.1 | ||
NM_001323615.1 | 296 | Intron | NP_001310544.1 | ||
NM_001323616.1 | 296 | Intron | NP_001310545.1 | ||
NM_001323617.1 | 296 | Intron | NP_001310546.1 | ||
NM_015327.2 | 296 | Intron | NP_056142.2 | ||
XM_017000842.1 | 296 | Intron | XP_016856331.1 | ||
XM_017000843.1 | 296 | Intron | XP_016856332.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032323.2 | 296 | Missense Mutation | CCG,CTG | P42L | NP_115699.1 |