ENST00000373344.11:c.4336G>C
MANE Select
|
ENSP00000362441.4:p.Glu1446Gln
|
|
ENST00000373344.9:c.4336G>C
|
ENSP00000362441.4:p.Glu1446Gln
|
|
ENST00000395603.7:c.4222G>C
|
ENSP00000378967.3:p.Glu1408Gln
|
|
ENST00000480283.5:c.*3964G>C
|
ENSP00000480196.1:n.*3964G>C
|
|
NM_000489.4:c.4336G>C
|
NP_000480.3:p.Glu1446Gln
|
|
NM_138270.3:c.4222G>C
|
NP_612114.2:p.Glu1408Gln
|
|
XM_005262153.3:c.4333G>C
|
XP_005262210.2:p.Glu1445Gln
|
|
XM_005262154.3:c.4249G>C
|
XP_005262211.2:p.Glu1417Gln
|
|
XM_005262155.3:c.4219G>C
|
XP_005262212.2:p.Glu1407Gln
|
|
XM_005262156.3:c.4171G>C
|
XP_005262213.2:p.Glu1391Gln
|
|
XM_005262157.3:c.4132G>C
|
XP_005262214.2:p.Glu1378Gln
|
|
XM_006724666.2:c.4219G>C
|
XP_006724729.1:p.Glu1407Gln
|
|
XM_006724667.2:c.4057G>C
|
XP_006724730.1:p.Glu1353Gln
|
|
XM_006724668.2:c.4336G>C
|
XP_006724731.1:p.Glu1446Gln
|
|
XR_938400.1:n.4604G>C
|
|
|
NM_000489.5:c.4336G>C
|
NP_000480.3:p.Glu1446Gln
|
|
XM_005262153.5:c.4333G>C
|
XP_005262210.2:p.Glu1445Gln
|
|
XM_005262154.5:c.4249G>C
|
XP_005262211.2:p.Glu1417Gln
|
|
XM_005262155.4:c.4219G>C
|
XP_005262212.2:p.Glu1407Gln
|
|
XM_005262156.4:c.4171G>C
|
XP_005262213.2:p.Glu1391Gln
|
|
XM_005262157.5:c.4132G>C
|
XP_005262214.2:p.Glu1378Gln
|
|
XM_006724666.4:c.4219G>C
|
XP_006724729.1:p.Glu1407Gln
|
|
XM_006724667.3:c.4057G>C
|
XP_006724730.1:p.Glu1353Gln
|
|
XM_006724668.3:c.4336G>C
|
XP_006724731.1:p.Glu1446Gln
|
|
XM_017029601.2:c.4246G>C
|
XP_016885090.1:p.Glu1416Gln
|
|
XM_017029602.1:c.4216G>C
|
XP_016885091.1:p.Glu1406Gln
|
|
XM_017029603.1:c.4168G>C
|
XP_016885092.1:p.Glu1390Gln
|
|
XM_017029604.2:c.4135G>C
|
XP_016885093.1:p.Glu1379Gln
|
|
XM_017029605.1:c.4132G>C
|
XP_016885094.1:p.Glu1378Gln
|
|
XM_017029606.2:c.4105G>C
|
XP_016885095.1:p.Glu1369Gln
|
|
XM_017029607.2:c.4102G>C
|
XP_016885096.1:p.Glu1368Gln
|
|
XM_017029608.2:c.4054G>C
|
XP_016885097.1:p.Glu1352Gln
|
|
XM_017029609.1:c.4018G>C
|
XP_016885098.1:p.Glu1340Gln
|
|
XM_017029610.1:c.4015G>C
|
XP_016885099.1:p.Glu1339Gln
|
|
XM_017029611.1:c.3970G>C
|
XP_016885100.1:p.Glu1324Gln
|
|
XR_001755700.2:n.4561G>C
|
|
|
NM_138270.4:c.4222G>C
|
NP_612114.2:p.Glu1408Gln
|
|
NM_000489.6:c.4336G>C
MANE Select
|
NP_000480.3:p.Glu1446Gln
|
|
NM_138270.5:c.4222G>C
|
NP_612114.2:p.Glu1408Gln
|
|