Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001006622.2 | 4167 | Intron | NP_001006623.1 | ||
NM_001006623.2 | 4167 | Intron | NP_001006624.1 | ||
NM_018383.4 | 4167 | Missense Mutation | CCG,CTG | P1323L | NP_060853.3 |
XM_005263697.2 | 4167 | UTR 3 | XP_005263754.1 | ||
XM_011511436.1 | 4167 | Missense Mutation | CCG,CTG | P1323L | XP_011509738.1 |
XM_017004435.1 | 4167 | Intron | XP_016859924.1 | ||
XM_017004436.1 | 4167 | Intron | XP_016859925.1 |