Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000269.2 | 303 | Intron | NP_000260.1 | ||
NM_198175.1 | 303 | Missense Mutation | CCT,CTT | P17L | NP_937818.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001018136.2 | 303 | Intron | NP_001018146.1 |