ENST00000378823.8:c.2637T>A
MANE Select
|
ENSP00000368100.4:p.Thr879=
|
|
ENST00000638452.2:c.2340T>A
|
ENSP00000492349.2:p.Thr780=
|
|
ENST00000638504.1:n.2245T>A
|
|
|
ENST00000638568.2:c.2340T>A
|
ENSP00000491158.2:p.Thr780=
|
|
ENST00000639899.1:n.3156T>A
|
|
|
ENST00000640655.2:c.2340T>A
|
ENSP00000491596.2:p.Thr780=
|
|
ENST00000651160.1:c.*781T>A
|
ENSP00000498829.1:n.*781T>A
|
|
ENST00000651723.1:c.*2720T>A
|
ENSP00000498237.1:n.*2720T>A
|
|
ENST00000652016.1:c.*854T>A
|
ENSP00000498267.1:n.*854T>A
|
|
ENST00000652485.1:c.2670T>A
|
ENSP00000498973.1:p.Thr890=
|
|
ENST00000378823.7:c.2637T>A
|
ENSP00000368100.4:p.Thr879=
|
|
ENST00000423956.5:c.*823T>A
|
ENSP00000390971.1:n.*823T>A
|
|
ENST00000533482.5:c.*2263T>A
|
ENSP00000431225.1:n.*2263T>A
|
|
NM_005732.3:c.2637T>A
|
NP_005723.2:p.Thr879=
|
|
NM_005732.4:c.2637T>A
MANE Select
|
NP_005723.2:p.Thr879=
|
|