Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003462.3 | 2138 | Intron | NP_003453.2 | ||
XM_005271172.2 | 2138 | Intron | XP_005271229.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001323623.1 | 2138 | Missense Mutation | CGG,TGG | R727W | NP_001310552.1 |
NM_001323624.1 | 2138 | Missense Mutation | CGG,TGG | R476W | NP_001310553.1 |
NM_013285.2 | 2138 | Missense Mutation | CGG,TGG | R659W | NP_037417.1 |