Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_013941.3 | 489 | Missense Mutation | CGG,TGG | R138W | NP_039229.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030876.5 | 489 | Intron | NP_110503.3 | ||
XM_011514929.2 | 489 | Intron | XP_011513231.1 | ||
XM_011514930.2 | 489 | Intron | XP_011513232.1 |