Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142603.2 | 4623 | Intron | NP_001136075.1 | ||
NM_014773.4 | 4623 | Intron | NP_055588.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016580.3 | 4623 | Missense Mutation | CGG,TGG | R1138W | NP_057664.1 |