ENST00000697149.1:c.1334A>G
|
ENSP00000513138.1:n.1334A>G
|
|
ENST00000697150.1:c.1392A>G
|
ENSP00000513139.1:n.1392A>G
|
|
ENST00000697151.1:c.1325A>G
|
ENSP00000513140.1:n.1325A>G
|
|
ENST00000697164.1:c.1405A>G
|
ENSP00000513153.1:p.Ser469Gly
|
|
ENST00000697165.1:c.1192A>G
|
ENSP00000513154.1:p.Ser398Gly
|
|
ENST00000347310.10:c.1495A>G
MANE Select
|
ENSP00000321345.5:p.Ser499Gly
|
|
ENST00000637002.1:c.886A>G
|
ENSP00000490340.1:p.Ser296Gly
|
|
ENST00000347310.9:c.1495A>G
|
ENSP00000321345.5:p.Ser499Gly
|
|
ENST00000395227.2:c.289A>G
|
ENSP00000378652.2:p.Ser97Gly
|
|
ENST00000425614.3:c.730A>G
|
ENSP00000387640.2:p.Ser244Gly
|
|
ENST00000473881.2:c.*321A>G
|
ENSP00000486667.1:n.*321A>G
|
|
NM_144701.2:c.1495A>G
|
NP_653302.2:p.Ser499Gly
|
|
XM_005270516.2:c.733A>G
|
XP_005270573.1:p.Ser245Gly
|
|
XM_011540789.1:c.1585A>G
|
XP_011539091.1:p.Ser529Gly
|
|
XM_011540790.1:c.1495A>G
|
XP_011539092.1:p.Ser499Gly
|
|
XM_011540791.1:c.1495A>G
|
XP_011539093.1:p.Ser499Gly
|
|
XM_011540790.3:c.1495A>G
|
XP_011539092.1:p.Ser499Gly
|
|
XM_011540791.3:c.1495A>G
|
XP_011539093.1:p.Ser499Gly
|
|
XR_001736993.1:n.1575A>G
|
|
|
NM_144701.3:c.1495A>G
MANE Select
|
NP_653302.2:p.Ser499Gly
|
|