ENST00000697149.1:c.1377T>A
|
ENSP00000513138.1:n.1377T>A
|
|
ENST00000697150.1:c.1435T>A
|
ENSP00000513139.1:n.1435T>A
|
|
ENST00000697151.1:c.1368T>A
|
ENSP00000513140.1:n.1368T>A
|
|
ENST00000697164.1:c.1448T>A
|
ENSP00000513153.1:p.Val483Asp
|
|
ENST00000697165.1:c.1235T>A
|
ENSP00000513154.1:p.Val412Asp
|
|
ENST00000347310.10:c.1538T>A
MANE Select
|
ENSP00000321345.5:p.Val513Asp
|
|
ENST00000637002.1:c.929T>A
|
ENSP00000490340.1:p.Val310Asp
|
|
ENST00000347310.9:c.1538T>A
|
ENSP00000321345.5:p.Val513Asp
|
|
ENST00000395227.2:c.332T>A
|
ENSP00000378652.2:p.Val111Asp
|
|
ENST00000425614.3:c.773T>A
|
ENSP00000387640.2:p.Val258Asp
|
|
ENST00000473881.2:c.*364T>A
|
ENSP00000486667.1:n.*364T>A
|
|
NM_144701.2:c.1538T>A
|
NP_653302.2:p.Val513Asp
|
|
XM_005270516.2:c.776T>A
|
XP_005270573.1:p.Val259Asp
|
|
XM_011540789.1:c.1628T>A
|
XP_011539091.1:p.Val543Asp
|
|
XM_011540790.1:c.1538T>A
|
XP_011539092.1:p.Val513Asp
|
|
XM_011540791.1:c.1538T>A
|
XP_011539093.1:p.Val513Asp
|
|
XM_011540790.3:c.1538T>A
|
XP_011539092.1:p.Val513Asp
|
|
XM_011540791.3:c.1538T>A
|
XP_011539093.1:p.Val513Asp
|
|
XR_001736993.1:n.1618T>A
|
|
|
NM_144701.3:c.1538T>A
MANE Select
|
NP_653302.2:p.Val513Asp
|
|