ENST00000378823.8:c.2071G=
MANE Select
|
ENSP00000368100.4:p.Glu691=
|
|
ENST00000638452.2:c.1774G=
|
ENSP00000492349.2:p.Glu592=
|
|
ENST00000638504.1:n.1679G=
|
|
|
ENST00000638568.2:c.1774G=
|
ENSP00000491158.2:p.Glu592=
|
|
ENST00000639899.1:n.2590G=
|
|
|
ENST00000640655.2:c.1774G=
|
ENSP00000491596.2:p.Glu592=
|
|
ENST00000651160.1:c.*215G=
|
ENSP00000498829.1:n.*215G=
|
|
ENST00000651658.1:n.2614G=
|
|
|
ENST00000651723.1:c.*2154G=
|
ENSP00000498237.1:n.*2154G=
|
|
ENST00000652016.1:c.*288G=
|
ENSP00000498267.1:n.*288G=
|
|
ENST00000652485.1:c.2104G=
|
ENSP00000498973.1:p.Glu702=
|
|
ENST00000378823.7:c.2071G=
|
ENSP00000368100.4:p.Glu691=
|
|
ENST00000423956.5:c.*257G=
|
ENSP00000390971.1:n.*257G=
|
|
ENST00000453394.5:c.1888G=
|
ENSP00000400049.1:p.Glu630=
|
|
ENST00000496204.1:n.154G=
|
|
|
ENST00000533482.5:c.*1697G=
|
ENSP00000431225.1:n.*1697G=
|
|
NM_005732.3:c.2071G=
|
NP_005723.2:p.Glu691=
|
|
NM_005732.4:c.2071G=
MANE Select
|
NP_005723.2:p.Glu691=
|
|