ENST00000697149.1:c.1332T>A
|
ENSP00000513138.1:n.1332T>A
|
|
ENST00000697150.1:c.1390T>A
|
ENSP00000513139.1:n.1390T>A
|
|
ENST00000697151.1:c.1323T>A
|
ENSP00000513140.1:n.1323T>A
|
|
ENST00000697164.1:c.1403T>A
|
ENSP00000513153.1:p.Leu468His
|
|
ENST00000697165.1:c.1190T>A
|
ENSP00000513154.1:p.Leu397His
|
|
ENST00000347310.10:c.1493T>A
MANE Select
|
ENSP00000321345.5:p.Leu498His
|
|
ENST00000637002.1:c.884T>A
|
ENSP00000490340.1:p.Leu295His
|
|
ENST00000347310.9:c.1493T>A
|
ENSP00000321345.5:p.Leu498His
|
|
ENST00000395227.2:c.287T>A
|
ENSP00000378652.2:p.Leu96His
|
|
ENST00000425614.3:c.728T>A
|
ENSP00000387640.2:p.Leu243His
|
|
ENST00000473881.2:c.*319T>A
|
ENSP00000486667.1:n.*319T>A
|
|
NM_144701.2:c.1493T>A
|
NP_653302.2:p.Leu498His
|
|
XM_005270516.2:c.731T>A
|
XP_005270573.1:p.Leu244His
|
|
XM_011540789.1:c.1583T>A
|
XP_011539091.1:p.Leu528His
|
|
XM_011540790.1:c.1493T>A
|
XP_011539092.1:p.Leu498His
|
|
XM_011540791.1:c.1493T>A
|
XP_011539093.1:p.Leu498His
|
|
XM_011540790.3:c.1493T>A
|
XP_011539092.1:p.Leu498His
|
|
XM_011540791.3:c.1493T>A
|
XP_011539093.1:p.Leu498His
|
|
XR_001736993.1:n.1573T>A
|
|
|
NM_144701.3:c.1493T>A
MANE Select
|
NP_653302.2:p.Leu498His
|
|