ENST00000378823.8:c.2642T>A
MANE Select
|
ENSP00000368100.4:p.Leu881Ter
|
|
ENST00000638452.2:c.2345T>A
|
ENSP00000492349.2:p.Leu782Ter
|
|
ENST00000638504.1:n.2250T>A
|
|
|
ENST00000638568.2:c.2345T>A
|
ENSP00000491158.2:p.Leu782Ter
|
|
ENST00000639899.1:n.3161T>A
|
|
|
ENST00000640655.2:c.2345T>A
|
ENSP00000491596.2:p.Leu782Ter
|
|
ENST00000651160.1:c.*786T>A
|
ENSP00000498829.1:n.*786T>A
|
|
ENST00000651723.1:c.*2725T>A
|
ENSP00000498237.1:n.*2725T>A
|
|
ENST00000652016.1:c.*859T>A
|
ENSP00000498267.1:n.*859T>A
|
|
ENST00000652485.1:c.2675T>A
|
ENSP00000498973.1:p.Leu892Ter
|
|
ENST00000378823.7:c.2642T>A
|
ENSP00000368100.4:p.Leu881Ter
|
|
ENST00000423956.5:c.*828T>A
|
ENSP00000390971.1:n.*828T>A
|
|
ENST00000533482.5:c.*2268T>A
|
ENSP00000431225.1:n.*2268T>A
|
|
NM_005732.3:c.2642T>A
|
NP_005723.2:p.Leu881Ter
|
|
NM_005732.4:c.2642T>A
MANE Select
|
NP_005723.2:p.Leu881Ter
|
|