Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001104.3 | 352 | Intron | NP_001095.2 | ||
NM_001258371.2 | 352 | Missense Mutation | CAG,CCG | Q79P | NP_001245300.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207340.1 | 352 | Intron | NP_997223.1 | ||
XM_005273874.3 | 352 | Intron | XP_005273931.1 | ||
XM_011544893.2 | 352 | Intron | XP_011543195.1 | ||
XM_011544894.1 | 352 | Intron | XP_011543196.1 |