Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144856.1 | 1631 | Intron | NP_001138328.1 | ||
NM_001144857.1 | 1631 | Intron | NP_001138329.1 | ||
NM_018173.3 | 1631 | Intron | NP_060643.2 | ||
XM_005253704.4 | 1631 | Intron | XP_005253761.1 | ||
XM_006718985.3 | 1631 | Intron | XP_006719048.1 | ||
XM_011520967.2 | 1631 | Intron | XP_011519269.1 | ||
XM_017019555.1 | 1631 | Intron | XP_016875044.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001065.3 | 1631 | Missense Mutation | GGC,GTC | G443V | NP_001056.1 |