ENST00000697149.1:c.1626C>A
|
ENSP00000513138.1:n.1626C>A
|
|
ENST00000697150.1:c.1684C>A
|
ENSP00000513139.1:n.1684C>A
|
|
ENST00000697151.1:c.1617C>A
|
ENSP00000513140.1:n.1617C>A
|
|
ENST00000697164.1:c.1697C>A
|
ENSP00000513153.1:p.Ser566Tyr
|
|
ENST00000697165.1:c.1484C>A
|
ENSP00000513154.1:p.Ser495Tyr
|
|
ENST00000347310.10:c.1787C>A
MANE Select
|
ENSP00000321345.5:p.Ser596Tyr
|
|
ENST00000637002.1:c.1178C>A
|
ENSP00000490340.1:p.Ser393Tyr
|
|
ENST00000347310.9:c.1787C>A
|
ENSP00000321345.5:p.Ser596Tyr
|
|
ENST00000395227.2:c.581C>A
|
ENSP00000378652.2:p.Ser194Tyr
|
|
ENST00000425614.3:c.1022C>A
|
ENSP00000387640.2:p.Ser341Tyr
|
|
ENST00000473881.2:c.*613C>A
|
ENSP00000486667.1:n.*613C>A
|
|
NM_144701.2:c.1787C>A
|
NP_653302.2:p.Ser596Tyr
|
|
XM_005270516.2:c.1025C>A
|
XP_005270573.1:p.Ser342Tyr
|
|
XM_011540789.1:c.1877C>A
|
XP_011539091.1:p.Ser626Tyr
|
|
XM_011540790.1:c.1787C>A
|
XP_011539092.1:p.Ser596Tyr
|
|
XM_011540791.1:c.1787C>A
|
XP_011539093.1:p.Ser596Tyr
|
|
XM_011540790.3:c.1787C>A
|
XP_011539092.1:p.Ser596Tyr
|
|
XM_011540791.3:c.1787C>A
|
XP_011539093.1:p.Ser596Tyr
|
|
XR_001736993.1:n.1867C>A
|
|
|
NM_144701.3:c.1787C>A
MANE Select
|
NP_653302.2:p.Ser596Tyr
|
|