ENST00000697149.1:c.1631T>A
|
ENSP00000513138.1:n.1631T>A
|
|
ENST00000697150.1:c.1689T>A
|
ENSP00000513139.1:n.1689T>A
|
|
ENST00000697151.1:c.1622T>A
|
ENSP00000513140.1:n.1622T>A
|
|
ENST00000697164.1:c.1702T>A
|
ENSP00000513153.1:p.Leu568Met
|
|
ENST00000697165.1:c.1489T>A
|
ENSP00000513154.1:p.Leu497Met
|
|
ENST00000347310.10:c.1792T>A
MANE Select
|
ENSP00000321345.5:p.Leu598Met
|
|
ENST00000637002.1:c.1183T>A
|
ENSP00000490340.1:p.Leu395Met
|
|
ENST00000347310.9:c.1792T>A
|
ENSP00000321345.5:p.Leu598Met
|
|
ENST00000395227.2:c.586T>A
|
ENSP00000378652.2:p.Leu196Met
|
|
ENST00000425614.3:c.1027T>A
|
ENSP00000387640.2:p.Leu343Met
|
|
ENST00000473881.2:c.*618T>A
|
ENSP00000486667.1:n.*618T>A
|
|
NM_144701.2:c.1792T>A
|
NP_653302.2:p.Leu598Met
|
|
XM_005270516.2:c.1030T>A
|
XP_005270573.1:p.Leu344Met
|
|
XM_011540789.1:c.1882T>A
|
XP_011539091.1:p.Leu628Met
|
|
XM_011540790.1:c.1792T>A
|
XP_011539092.1:p.Leu598Met
|
|
XM_011540791.1:c.1792T>A
|
XP_011539093.1:p.Leu598Met
|
|
XM_011540790.3:c.1792T>A
|
XP_011539092.1:p.Leu598Met
|
|
XM_011540791.3:c.1792T>A
|
XP_011539093.1:p.Leu598Met
|
|
XR_001736993.1:n.1872T>A
|
|
|
NM_144701.3:c.1792T>A
MANE Select
|
NP_653302.2:p.Leu598Met
|
|