Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256295.1 | 162 | Missense Mutation | CAA,CCA | Q41P | NP_001243224.1 |
NM_005239.5 | 162 | Intron | NP_005230.1 | ||
XM_005260935.1 | 162 | Intron | XP_005260992.1 | ||
XM_017028290.1 | 162 | Intron | XP_016883779.1 |