ENST00000378823.8:c.2673T>C
MANE Select
|
ENSP00000368100.4:p.Thr891=
|
|
ENST00000638452.2:c.2376T>C
|
ENSP00000492349.2:p.Thr792=
|
|
ENST00000638504.1:n.2281T>C
|
|
|
ENST00000638568.2:c.2376T>C
|
ENSP00000491158.2:p.Thr792=
|
|
ENST00000639899.1:n.3192T>C
|
|
|
ENST00000640655.2:c.2376T>C
|
ENSP00000491596.2:p.Thr792=
|
|
ENST00000651160.1:c.*817T>C
|
ENSP00000498829.1:n.*817T>C
|
|
ENST00000651723.1:c.*2756T>C
|
ENSP00000498237.1:n.*2756T>C
|
|
ENST00000652016.1:c.*890T>C
|
ENSP00000498267.1:n.*890T>C
|
|
ENST00000378823.7:c.2673T>C
|
ENSP00000368100.4:p.Thr891=
|
|
ENST00000423956.5:c.*859T>C
|
ENSP00000390971.1:n.*859T>C
|
|
ENST00000533482.5:c.*2299T>C
|
ENSP00000431225.1:n.*2299T>C
|
|
NM_005732.3:c.2673T>C
|
NP_005723.2:p.Thr891=
|
|
NM_005732.4:c.2673T>C
MANE Select
|
NP_005723.2:p.Thr891=
|
|