Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001270396.1 | 71 | Missense Mutation | CCC,TCC | P15S | NP_001257325.1 |
NM_152436.2 | 71 | Missense Mutation | CCC,TCC | P15S | NP_689649.1 |
XM_011537949.2 | 71 | UTR 5 | XP_011536251.1 | ||
XM_011537950.2 | 71 | Intron | XP_011536252.1 | ||
XM_017018848.1 | 71 | Intron | XP_016874337.1 | ||
XM_017018849.1 | 71 | Intron | XP_016874338.1 |