ENST00000373344.11:c.4352A>G
MANE Select
|
ENSP00000362441.4:p.Glu1451Gly
|
|
ENST00000373344.9:c.4352A>G
|
ENSP00000362441.4:p.Glu1451Gly
|
|
ENST00000395603.7:c.4238A>G
|
ENSP00000378967.3:p.Glu1413Gly
|
|
ENST00000480283.5:c.*3980A>G
|
ENSP00000480196.1:n.*3980A>G
|
|
NM_000489.4:c.4352A>G
|
NP_000480.3:p.Glu1451Gly
|
|
NM_138270.3:c.4238A>G
|
NP_612114.2:p.Glu1413Gly
|
|
XM_005262153.3:c.4349A>G
|
XP_005262210.2:p.Glu1450Gly
|
|
XM_005262154.3:c.4265A>G
|
XP_005262211.2:p.Glu1422Gly
|
|
XM_005262155.3:c.4235A>G
|
XP_005262212.2:p.Glu1412Gly
|
|
XM_005262156.3:c.4187A>G
|
XP_005262213.2:p.Glu1396Gly
|
|
XM_005262157.3:c.4148A>G
|
XP_005262214.2:p.Glu1383Gly
|
|
XM_006724666.2:c.4235A>G
|
XP_006724729.1:p.Glu1412Gly
|
|
XM_006724667.2:c.4073A>G
|
XP_006724730.1:p.Glu1358Gly
|
|
XM_006724668.2:c.4352A>G
|
XP_006724731.1:p.Glu1451Gly
|
|
XR_938400.1:n.4620A>G
|
|
|
NM_000489.5:c.4352A>G
|
NP_000480.3:p.Glu1451Gly
|
|
XM_005262153.5:c.4349A>G
|
XP_005262210.2:p.Glu1450Gly
|
|
XM_005262154.5:c.4265A>G
|
XP_005262211.2:p.Glu1422Gly
|
|
XM_005262155.4:c.4235A>G
|
XP_005262212.2:p.Glu1412Gly
|
|
XM_005262156.4:c.4187A>G
|
XP_005262213.2:p.Glu1396Gly
|
|
XM_005262157.5:c.4148A>G
|
XP_005262214.2:p.Glu1383Gly
|
|
XM_006724666.4:c.4235A>G
|
XP_006724729.1:p.Glu1412Gly
|
|
XM_006724667.3:c.4073A>G
|
XP_006724730.1:p.Glu1358Gly
|
|
XM_006724668.3:c.4352A>G
|
XP_006724731.1:p.Glu1451Gly
|
|
XM_017029601.2:c.4262A>G
|
XP_016885090.1:p.Glu1421Gly
|
|
XM_017029602.1:c.4232A>G
|
XP_016885091.1:p.Glu1411Gly
|
|
XM_017029603.1:c.4184A>G
|
XP_016885092.1:p.Glu1395Gly
|
|
XM_017029604.2:c.4151A>G
|
XP_016885093.1:p.Glu1384Gly
|
|
XM_017029605.1:c.4148A>G
|
XP_016885094.1:p.Glu1383Gly
|
|
XM_017029606.2:c.4121A>G
|
XP_016885095.1:p.Glu1374Gly
|
|
XM_017029607.2:c.4118A>G
|
XP_016885096.1:p.Glu1373Gly
|
|
XM_017029608.2:c.4070A>G
|
XP_016885097.1:p.Glu1357Gly
|
|
XM_017029609.1:c.4034A>G
|
XP_016885098.1:p.Glu1345Gly
|
|
XM_017029610.1:c.4031A>G
|
XP_016885099.1:p.Glu1344Gly
|
|
XM_017029611.1:c.3986A>G
|
XP_016885100.1:p.Glu1329Gly
|
|
XR_001755700.2:n.4577A>G
|
|
|
NM_138270.4:c.4238A>G
|
NP_612114.2:p.Glu1413Gly
|
|
NM_000489.6:c.4352A>G
MANE Select
|
NP_000480.3:p.Glu1451Gly
|
|
NM_138270.5:c.4238A>G
|
NP_612114.2:p.Glu1413Gly
|
|