Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002918.1 | 467 | Missense Mutation | GCC,GTC | A156V | NP_001002918.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005198.1 | 467 | Intron | NP_001005198.1 | ||
XM_011542662.2 | 467 | Intron | XP_011540964.1 | ||
XM_011542663.2 | 467 | Intron | XP_011540965.1 | ||
XM_011542664.2 | 467 | Intron | XP_011540966.1 | ||
XM_011542665.2 | 467 | Intron | XP_011540967.1 | ||
XM_011542666.2 | 467 | Intron | XP_011540968.1 | ||
XM_011542667.2 | 467 | Intron | XP_011540969.1 |