Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030785.3 | 3785 | Intron | NP_110412.1 | ||
XM_011527351.1 | 3785 | Intron | XP_011525653.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004819.2 | 3785 | Missense Mutation | CCT,CTT | P1196L | NP_004810.2 |
XM_005259286.1 | 3785 | Missense Mutation | CCT,CTT | P1196L | XP_005259343.1 |
XM_011527354.1 | 3785 | Missense Mutation | CCT,CTT | P1196L | XP_011525656.1 |