ENST00000378823.8:c.566T>A
MANE Select
|
ENSP00000368100.4:p.Leu189Ter
|
|
ENST00000638452.2:c.269T>A
|
ENSP00000492349.2:p.Leu90Ter
|
|
ENST00000638504.1:n.442+3948T>A
|
|
|
ENST00000638568.2:c.269T>A
|
ENSP00000491158.2:p.Leu90Ter
|
|
ENST00000639899.1:n.1085T>A
|
|
|
ENST00000640655.2:c.269T>A
|
ENSP00000491596.2:p.Leu90Ter
|
|
ENST00000651160.1:c.566T>A
|
ENSP00000498829.1:p.Leu189Ter
|
|
ENST00000651541.1:c.269T>A
|
ENSP00000498795.1:p.Leu90Ter
|
|
ENST00000651658.1:n.993T>A
|
|
|
ENST00000651723.1:c.*649T>A
|
ENSP00000498237.1:n.*649T>A
|
|
ENST00000652016.1:c.566T>A
|
ENSP00000498267.1:p.Leu189Ter
|
|
ENST00000652485.1:c.566T>A
|
ENSP00000498973.1:p.Leu189Ter
|
|
ENST00000378823.7:c.566T>A
|
ENSP00000368100.4:p.Leu189Ter
|
|
ENST00000416135.5:c.269T>A
|
ENSP00000389515.1:p.Leu90Ter
|
|
ENST00000423956.5:c.566T>A
|
ENSP00000390971.1:p.Leu189Ter
|
|
ENST00000453394.5:c.566T>A
|
ENSP00000400049.1:p.Leu189Ter
|
|
ENST00000487596.1:n.132T>A
|
|
|
ENST00000533482.5:c.*192T>A
|
ENSP00000431225.1:n.*192T>A
|
|
NM_005732.3:c.566T>A
|
NP_005723.2:p.Leu189Ter
|
|
NM_005732.4:c.566T>A
MANE Select
|
NP_005723.2:p.Leu189Ter
|
|