Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014335.2 | 169 | Missense Mutation | CCG,TCG | P29S | NP_055150.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_203349.3 | 169 | Intron | NP_976224.3 | ||
XM_005254375.3 | 169 | Intron | XP_005254432.1 |