ENST00000378823.8:c.1893T>G
MANE Select
|
ENSP00000368100.4:p.Asp631Glu
|
|
ENST00000638452.2:c.1596T>G
|
ENSP00000492349.2:p.Asp532Glu
|
|
ENST00000638504.1:n.1480-136T>G
|
|
|
ENST00000638568.2:c.1596T>G
|
ENSP00000491158.2:p.Asp532Glu
|
|
ENST00000639899.1:n.2412T>G
|
|
|
ENST00000640655.2:c.1596T>G
|
ENSP00000491596.2:p.Asp532Glu
|
|
ENST00000651160.1:c.*16-136T>G
|
ENSP00000498829.1:n.*16-136T>G
|
|
ENST00000651658.1:n.2436T>G
|
|
|
ENST00000651723.1:c.*1976T>G
|
ENSP00000498237.1:n.*1976T>G
|
|
ENST00000652016.1:c.*89-136T>G
|
ENSP00000498267.1:n.*89-136T>G
|
|
ENST00000652485.1:c.1926T>G
|
ENSP00000498973.1:p.Asp642Glu
|
|
ENST00000378823.7:c.1893T>G
|
ENSP00000368100.4:p.Asp631Glu
|
|
ENST00000423956.5:c.*79T>G
|
ENSP00000390971.1:n.*79T>G
|
|
ENST00000453394.5:c.1710T>G
|
ENSP00000400049.1:p.Asp570Glu
|
|
ENST00000533482.5:c.*1519T>G
|
ENSP00000431225.1:n.*1519T>G
|
|
NM_005732.3:c.1893T>G
|
NP_005723.2:p.Asp631Glu
|
|
NM_005732.4:c.1893T>G
MANE Select
|
NP_005723.2:p.Asp631Glu
|
|