ENST00000378823.8:c.1840G>T
MANE Select
|
ENSP00000368100.4:p.Glu614Ter
|
|
ENST00000638452.2:c.1543G>T
|
ENSP00000492349.2:p.Glu515Ter
|
|
ENST00000638504.1:n.1480-189G>T
|
|
|
ENST00000638568.2:c.1543G>T
|
ENSP00000491158.2:p.Glu515Ter
|
|
ENST00000639899.1:n.2359G>T
|
|
|
ENST00000640655.2:c.1543G>T
|
ENSP00000491596.2:p.Glu515Ter
|
|
ENST00000651160.1:c.*16-189G>T
|
ENSP00000498829.1:n.*16-189G>T
|
|
ENST00000651658.1:n.2383G>T
|
|
|
ENST00000651723.1:c.*1923G>T
|
ENSP00000498237.1:n.*1923G>T
|
|
ENST00000652016.1:c.*89-189G>T
|
ENSP00000498267.1:n.*89-189G>T
|
|
ENST00000652485.1:c.1873G>T
|
ENSP00000498973.1:p.Glu625Ter
|
|
ENST00000378823.7:c.1840G>T
|
ENSP00000368100.4:p.Glu614Ter
|
|
ENST00000423956.5:c.*26G>T
|
ENSP00000390971.1:n.*26G>T
|
|
ENST00000453394.5:c.1657G>T
|
ENSP00000400049.1:p.Glu553Ter
|
|
ENST00000533482.5:c.*1466G>T
|
ENSP00000431225.1:n.*1466G>T
|
|
NM_005732.3:c.1840G>T
|
NP_005723.2:p.Glu614Ter
|
|
NM_005732.4:c.1840G>T
MANE Select
|
NP_005723.2:p.Glu614Ter
|
|