Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004869.3 | 1413 | Missense Mutation | CCT,TCT | P385S | NP_004860.2 |
XM_006722582.2 | 1413 | Missense Mutation | CCT,TCT | P267S | XP_006722645.1 |
XM_011526268.2 | 1413 | Missense Mutation | CCT,TCT | P385S | XP_011524570.1 |