Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304349.1 | 1679 | Missense Mutation | CCT,TCT | P425S | NP_001291278.1 |
NM_002730.3 | 1679 | Missense Mutation | CCT,TCT | P349S | NP_002721.1 |
NM_207518.2 | 1679 | Intron | NP_997401.1 | ||
XM_017026948.1 | 1679 | Intron | XP_016882437.1 |