ENST00000378823.8:c.2088A=
MANE Select
|
ENSP00000368100.4:p.Glu696=
|
|
ENST00000638452.2:c.1791A=
|
ENSP00000492349.2:p.Glu597=
|
|
ENST00000638504.1:n.1696A=
|
|
|
ENST00000638568.2:c.1791A=
|
ENSP00000491158.2:p.Glu597=
|
|
ENST00000639899.1:n.2607A=
|
|
|
ENST00000640655.2:c.1791A=
|
ENSP00000491596.2:p.Glu597=
|
|
ENST00000651160.1:c.*232A=
|
ENSP00000498829.1:n.*232A=
|
|
ENST00000651658.1:n.2631A=
|
|
|
ENST00000651723.1:c.*2171A=
|
ENSP00000498237.1:n.*2171A=
|
|
ENST00000652016.1:c.*305A=
|
ENSP00000498267.1:n.*305A=
|
|
ENST00000652485.1:c.2121A=
|
ENSP00000498973.1:p.Glu707=
|
|
ENST00000378823.7:c.2088A=
|
ENSP00000368100.4:p.Glu696=
|
|
ENST00000423956.5:c.*274A=
|
ENSP00000390971.1:n.*274A=
|
|
ENST00000453394.5:c.1905A=
|
ENSP00000400049.1:p.Glu635=
|
|
ENST00000496204.1:n.171A=
|
|
|
ENST00000533482.5:c.*1714A=
|
ENSP00000431225.1:n.*1714A=
|
|
NM_005732.3:c.2088A=
|
NP_005723.2:p.Glu696=
|
|
NM_005732.4:c.2088A=
MANE Select
|
NP_005723.2:p.Glu696=
|
|