ENST00000697149.1:c.1456A>T
|
ENSP00000513138.1:n.1456A>T
|
|
ENST00000697150.1:c.1514A>T
|
ENSP00000513139.1:n.1514A>T
|
|
ENST00000697151.1:c.1447A>T
|
ENSP00000513140.1:n.1447A>T
|
|
ENST00000697164.1:c.1527A>T
|
ENSP00000513153.1:p.Ser509=
|
|
ENST00000697165.1:c.1314A>T
|
ENSP00000513154.1:p.Ser438=
|
|
ENST00000347310.10:c.1617A>T
MANE Select
|
ENSP00000321345.5:p.Ser539=
|
|
ENST00000637002.1:c.1008A>T
|
ENSP00000490340.1:p.Ser336=
|
|
ENST00000347310.9:c.1617A>T
|
ENSP00000321345.5:p.Ser539=
|
|
ENST00000395227.2:c.411A>T
|
ENSP00000378652.2:p.Ser137=
|
|
ENST00000425614.3:c.852A>T
|
ENSP00000387640.2:p.Ser284=
|
|
ENST00000473881.2:c.*443A>T
|
ENSP00000486667.1:n.*443A>T
|
|
NM_144701.2:c.1617A>T
|
NP_653302.2:p.Ser539=
|
|
XM_005270516.2:c.855A>T
|
XP_005270573.1:p.Ser285=
|
|
XM_011540789.1:c.1707A>T
|
XP_011539091.1:p.Ser569=
|
|
XM_011540790.1:c.1617A>T
|
XP_011539092.1:p.Ser539=
|
|
XM_011540791.1:c.1617A>T
|
XP_011539093.1:p.Ser539=
|
|
XM_011540790.3:c.1617A>T
|
XP_011539092.1:p.Ser539=
|
|
XM_011540791.3:c.1617A>T
|
XP_011539093.1:p.Ser539=
|
|
XR_001736993.1:n.1697A>T
|
|
|
NM_144701.3:c.1617A>T
MANE Select
|
NP_653302.2:p.Ser539=
|
|