ENST00000644719.2:c.741G>C
MANE Select
|
ENSP00000496625.1:p.Glu247Asp
|
|
ENST00000418967.6:c.741G>C
|
ENSP00000408860.2:p.Glu247Asp
|
|
ENST00000435122.3:c.651G>C
|
ENSP00000415043.2:p.Glu217Asp
|
|
ENST00000479074.5:n.799G>C
|
|
|
ENST00000479730.5:n.857G>C
|
|
|
ENST00000483041.5:n.910G>C
|
|
|
ENST00000486063.5:n.918+172G>C
|
|
|
NM_000500.7:c.741G>C
|
NP_000491.4:p.Glu247Asp
|
|
NM_001128590.3:c.651G>C
|
NP_001122062.3:p.Glu217Asp
|
|
XM_011514314.1:c.336G>C
|
XP_011512616.1:p.Glu112Asp
|
|
NM_000500.9:c.741G>C
MANE Select
|
NP_000491.4:p.Glu247Asp
|
|
NM_001368143.1:c.336G>C
|
NP_001355072.1:p.Glu112Asp
|
|
NM_001368144.1:c.336G>C
|
NP_001355073.1:p.Glu112Asp
|
|
NM_001128590.4:c.651G>C
|
NP_001122062.3:p.Glu217Asp
|
|
NM_001368143.2:c.336G>C
|
NP_001355072.1:p.Glu112Asp
|
|
NM_001368144.2:c.336G>C
|
NP_001355073.1:p.Glu112Asp
|
|