Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001788.3 | 1083 | Missense Mutation | GCC,GTC | A314V | NP_001001788.2 |
XM_011535800.2 | 1083 | Intron | XP_011534102.1 | ||
XM_017010831.1 | 1083 | Intron | XP_016866320.1 |