ENST00000378823.8:c.2501A>T
MANE Select
|
ENSP00000368100.4:p.Glu834Val
|
|
ENST00000638452.2:c.2204A>T
|
ENSP00000492349.2:p.Glu735Val
|
|
ENST00000638504.1:n.2109A>T
|
|
|
ENST00000638568.2:c.2204A>T
|
ENSP00000491158.2:p.Glu735Val
|
|
ENST00000639899.1:n.3020A>T
|
|
|
ENST00000640655.2:c.2204A>T
|
ENSP00000491596.2:p.Glu735Val
|
|
ENST00000651160.1:c.*645A>T
|
ENSP00000498829.1:n.*645A>T
|
|
ENST00000651658.1:n.3044A>T
|
|
|
ENST00000651723.1:c.*2584A>T
|
ENSP00000498237.1:n.*2584A>T
|
|
ENST00000652016.1:c.*718A>T
|
ENSP00000498267.1:n.*718A>T
|
|
ENST00000652485.1:c.2534A>T
|
ENSP00000498973.1:p.Glu845Val
|
|
ENST00000378823.7:c.2501A>T
|
ENSP00000368100.4:p.Glu834Val
|
|
ENST00000423956.5:c.*687A>T
|
ENSP00000390971.1:n.*687A>T
|
|
ENST00000533482.5:c.*2127A>T
|
ENSP00000431225.1:n.*2127A>T
|
|
NM_005732.3:c.2501A>T
|
NP_005723.2:p.Glu834Val
|
|
NM_005732.4:c.2501A>T
MANE Select
|
NP_005723.2:p.Glu834Val
|
|