ENST00000697149.1:c.1574T>A
|
ENSP00000513138.1:n.1574T>A
|
|
ENST00000697150.1:c.1632T>A
|
ENSP00000513139.1:n.1632T>A
|
|
ENST00000697151.1:c.1565T>A
|
ENSP00000513140.1:n.1565T>A
|
|
ENST00000697164.1:c.1645T>A
|
ENSP00000513153.1:p.Ser549Thr
|
|
ENST00000697165.1:c.1432T>A
|
ENSP00000513154.1:p.Ser478Thr
|
|
ENST00000347310.10:c.1735T>A
MANE Select
|
ENSP00000321345.5:p.Ser579Thr
|
|
ENST00000637002.1:c.1126T>A
|
ENSP00000490340.1:p.Ser376Thr
|
|
ENST00000347310.9:c.1735T>A
|
ENSP00000321345.5:p.Ser579Thr
|
|
ENST00000395227.2:c.529T>A
|
ENSP00000378652.2:p.Ser177Thr
|
|
ENST00000425614.3:c.970T>A
|
ENSP00000387640.2:p.Ser324Thr
|
|
ENST00000473881.2:c.*561T>A
|
ENSP00000486667.1:n.*561T>A
|
|
NM_144701.2:c.1735T>A
|
NP_653302.2:p.Ser579Thr
|
|
XM_005270516.2:c.973T>A
|
XP_005270573.1:p.Ser325Thr
|
|
XM_011540789.1:c.1825T>A
|
XP_011539091.1:p.Ser609Thr
|
|
XM_011540790.1:c.1735T>A
|
XP_011539092.1:p.Ser579Thr
|
|
XM_011540791.1:c.1735T>A
|
XP_011539093.1:p.Ser579Thr
|
|
XM_011540790.3:c.1735T>A
|
XP_011539092.1:p.Ser579Thr
|
|
XM_011540791.3:c.1735T>A
|
XP_011539093.1:p.Ser579Thr
|
|
XR_001736993.1:n.1815T>A
|
|
|
NM_144701.3:c.1735T>A
MANE Select
|
NP_653302.2:p.Ser579Thr
|
|