Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001159642.1 | 723 | Missense Mutation | CCT,TCT | P18S | NP_001153114.1 |
NM_138278.3 | 723 | Missense Mutation | CCT,TCT | P100S | NP_612122.2 |
XM_011509236.1 | 723 | Missense Mutation | CCT,TCT | P100S | XP_011507538.1 |
XM_017000420.1 | 723 | Intron | XP_016855909.1 |