Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000164.3 | 562 | Missense Mutation | CGG,TGG | R136W | NP_000155.1 |
NM_001308418.1 | 562 | Missense Mutation | CGG,TGG | R100W | NP_001295347.1 |
XM_011526709.2 | 562 | Missense Mutation | CGG,TGG | R136W | XP_011525011.1 |
XM_011526710.2 | 562 | Missense Mutation | CGG,TGG | R136W | XP_011525012.1 |
XM_011526711.2 | 562 | Missense Mutation | CGG,TGG | R100W | XP_011525013.1 |
XM_011526713.2 | 562 | Intron | XP_011525015.1 | ||
XM_011526714.2 | 562 | UTR 5 | XP_011525016.1 | ||
XM_011526715.2 | 562 | UTR 5 | XP_011525017.1 | ||
XM_011526716.2 | 562 | Missense Mutation | CGG,TGG | R136W | XP_011525018.1 |
XM_017026584.1 | 562 | Intron | XP_016882073.1 | ||
XM_017026585.1 | 562 | Intron | XP_016882074.1 | ||
XM_017026586.1 | 562 | Intron | XP_016882075.1 | ||
XM_017026587.1 | 562 | Intron | XP_016882076.1 |