Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001200029.1 | 399 | Intron | NP_001186958.1 | ||
NM_001200030.1 | 399 | Intron | NP_001186959.1 | ||
NM_001200031.1 | 399 | Intron | NP_001186960.1 | ||
NM_001200032.1 | 399 | Intron | NP_001186961.1 | ||
NM_003549.3 | 399 | Intron | NP_003540.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001200016.1 | 399 | Missense Mutation | TCC,TTC | S89F | NP_001186945.1 |
NM_001200018.1 | 399 | Missense Mutation | TCC,TTC | S89F | NP_001186947.1 |
NM_012191.3 | 399 | Missense Mutation | TCC,TTC | S111F | NP_036323.2 |