ENST00000373344.11:c.4394A>T
MANE Select
|
ENSP00000362441.4:p.Asp1465Val
|
|
ENST00000373344.9:c.4394A>T
|
ENSP00000362441.4:p.Asp1465Val
|
|
ENST00000395603.7:c.4280A>T
|
ENSP00000378967.3:p.Asp1427Val
|
|
ENST00000480283.5:c.*4022A>T
|
ENSP00000480196.1:n.*4022A>T
|
|
NM_000489.4:c.4394A>T
|
NP_000480.3:p.Asp1465Val
|
|
NM_138270.3:c.4280A>T
|
NP_612114.2:p.Asp1427Val
|
|
XM_005262153.3:c.4391A>T
|
XP_005262210.2:p.Asp1464Val
|
|
XM_005262154.3:c.4307A>T
|
XP_005262211.2:p.Asp1436Val
|
|
XM_005262155.3:c.4277A>T
|
XP_005262212.2:p.Asp1426Val
|
|
XM_005262156.3:c.4229A>T
|
XP_005262213.2:p.Asp1410Val
|
|
XM_005262157.3:c.4190A>T
|
XP_005262214.2:p.Asp1397Val
|
|
XM_006724666.2:c.4277A>T
|
XP_006724729.1:p.Asp1426Val
|
|
XM_006724667.2:c.4115A>T
|
XP_006724730.1:p.Asp1372Val
|
|
XM_006724668.2:c.4394A>T
|
XP_006724731.1:p.Asp1465Val
|
|
XR_938400.1:n.4662A>T
|
|
|
NM_000489.5:c.4394A>T
|
NP_000480.3:p.Asp1465Val
|
|
XM_005262153.5:c.4391A>T
|
XP_005262210.2:p.Asp1464Val
|
|
XM_005262154.5:c.4307A>T
|
XP_005262211.2:p.Asp1436Val
|
|
XM_005262155.4:c.4277A>T
|
XP_005262212.2:p.Asp1426Val
|
|
XM_005262156.4:c.4229A>T
|
XP_005262213.2:p.Asp1410Val
|
|
XM_005262157.5:c.4190A>T
|
XP_005262214.2:p.Asp1397Val
|
|
XM_006724666.4:c.4277A>T
|
XP_006724729.1:p.Asp1426Val
|
|
XM_006724667.3:c.4115A>T
|
XP_006724730.1:p.Asp1372Val
|
|
XM_006724668.3:c.4394A>T
|
XP_006724731.1:p.Asp1465Val
|
|
XM_017029601.2:c.4304A>T
|
XP_016885090.1:p.Asp1435Val
|
|
XM_017029602.1:c.4274A>T
|
XP_016885091.1:p.Asp1425Val
|
|
XM_017029603.1:c.4226A>T
|
XP_016885092.1:p.Asp1409Val
|
|
XM_017029604.2:c.4193A>T
|
XP_016885093.1:p.Asp1398Val
|
|
XM_017029605.1:c.4190A>T
|
XP_016885094.1:p.Asp1397Val
|
|
XM_017029606.2:c.4163A>T
|
XP_016885095.1:p.Asp1388Val
|
|
XM_017029607.2:c.4160A>T
|
XP_016885096.1:p.Asp1387Val
|
|
XM_017029608.2:c.4112A>T
|
XP_016885097.1:p.Asp1371Val
|
|
XM_017029609.1:c.4076A>T
|
XP_016885098.1:p.Asp1359Val
|
|
XM_017029610.1:c.4073A>T
|
XP_016885099.1:p.Asp1358Val
|
|
XM_017029611.1:c.4028A>T
|
XP_016885100.1:p.Asp1343Val
|
|
XR_001755700.2:n.4619A>T
|
|
|
NM_138270.4:c.4280A>T
|
NP_612114.2:p.Asp1427Val
|
|
NM_000489.6:c.4394A>T
MANE Select
|
NP_000480.3:p.Asp1465Val
|
|
NM_138270.5:c.4280A>T
|
NP_612114.2:p.Asp1427Val
|
|