Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014611.2 | 16646 | Missense Mutation | CCT,TCT | P5552S | NP_055426.1 |
XM_005248700.3 | 16646 | Missense Mutation | CCT,TCT | P3547S | XP_005248757.1 |
XM_006715405.3 | 16646 | Missense Mutation | CCT,TCT | P3700S | XP_006715468.1 |
XM_011535635.2 | 16646 | Missense Mutation | CCT,TCT | P5455S | XP_011533937.1 |
XM_011535636.2 | 16646 | Intron | XP_011533938.1 |