ENST00000697149.1:c.1641T>A
|
ENSP00000513138.1:n.1641T>A
|
|
ENST00000697150.1:c.1699T>A
|
ENSP00000513139.1:n.1699T>A
|
|
ENST00000697151.1:c.1632T>A
|
ENSP00000513140.1:n.1632T>A
|
|
ENST00000697164.1:c.1712T>A
|
ENSP00000513153.1:p.Val571Glu
|
|
ENST00000697165.1:c.1499T>A
|
ENSP00000513154.1:p.Val500Glu
|
|
ENST00000347310.10:c.1802T>A
MANE Select
|
ENSP00000321345.5:p.Val601Glu
|
|
ENST00000637002.1:c.1193T>A
|
ENSP00000490340.1:p.Val398Glu
|
|
ENST00000347310.9:c.1802T>A
|
ENSP00000321345.5:p.Val601Glu
|
|
ENST00000395227.2:c.596T>A
|
ENSP00000378652.2:p.Val199Glu
|
|
ENST00000425614.3:c.1037T>A
|
ENSP00000387640.2:p.Val346Glu
|
|
ENST00000473881.2:c.*628T>A
|
ENSP00000486667.1:n.*628T>A
|
|
NM_144701.2:c.1802T>A
|
NP_653302.2:p.Val601Glu
|
|
XM_005270516.2:c.1040T>A
|
XP_005270573.1:p.Val347Glu
|
|
XM_011540789.1:c.1892T>A
|
XP_011539091.1:p.Val631Glu
|
|
XM_011540790.1:c.1802T>A
|
XP_011539092.1:p.Val601Glu
|
|
XM_011540791.1:c.1802T>A
|
XP_011539093.1:p.Val601Glu
|
|
XM_011540790.3:c.1802T>A
|
XP_011539092.1:p.Val601Glu
|
|
XM_011540791.3:c.1802T>A
|
XP_011539093.1:p.Val601Glu
|
|
XR_001736993.1:n.1882T>A
|
|
|
NM_144701.3:c.1802T>A
MANE Select
|
NP_653302.2:p.Val601Glu
|
|