Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289934.1 | 2057 | Intron | NP_001276863.1 | ||
NM_002319.4 | 2057 | Missense Mutation | CCT,TCT | P657S | NP_002310.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289933.1 | 2057 | Intron | NP_001276862.1 |