Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001159642.1 | 598 | Intron | NP_001153114.1 | ||
NM_138278.3 | 598 | Intron | NP_612122.2 | ||
XM_011509236.1 | 598 | Intron | XP_011507538.1 | ||
XM_017000420.1 | 598 | Intron | XP_016855909.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017860.3 | 598 | Missense Mutation | CCT,CTT | P178L | NP_060330.2 |