ENST00000378823.8:c.1813G>T
MANE Select
|
ENSP00000368100.4:p.Glu605Ter
|
|
ENST00000638452.2:c.1516G>T
|
ENSP00000492349.2:p.Glu506Ter
|
|
ENST00000638504.1:n.1480-216G>T
|
|
|
ENST00000638568.2:c.1516G>T
|
ENSP00000491158.2:p.Glu506Ter
|
|
ENST00000639899.1:n.2332G>T
|
|
|
ENST00000640655.2:c.1516G>T
|
ENSP00000491596.2:p.Glu506Ter
|
|
ENST00000651160.1:c.*16-216G>T
|
ENSP00000498829.1:n.*16-216G>T
|
|
ENST00000651658.1:n.2356G>T
|
|
|
ENST00000651723.1:c.*1896G>T
|
ENSP00000498237.1:n.*1896G>T
|
|
ENST00000652016.1:c.*88+211G>T
|
ENSP00000498267.1:n.*88+211G>T
|
|
ENST00000652485.1:c.1846G>T
|
ENSP00000498973.1:p.Glu616Ter
|
|
ENST00000378823.7:c.1813G>T
|
ENSP00000368100.4:p.Glu605Ter
|
|
ENST00000423956.5:c.1655G>T
|
ENSP00000390971.1:p.Ter552Leu
|
|
ENST00000453394.5:c.1630G>T
|
ENSP00000400049.1:p.Glu544Ter
|
|
ENST00000533482.5:c.*1439G>T
|
ENSP00000431225.1:n.*1439G>T
|
|
NM_005732.3:c.1813G>T
|
NP_005723.2:p.Glu605Ter
|
|
NM_005732.4:c.1813G>T
MANE Select
|
NP_005723.2:p.Glu605Ter
|
|