ENST00000373344.11:c.4388A>C
MANE Select
|
ENSP00000362441.4:p.Glu1463Ala
|
|
ENST00000373344.9:c.4388A>C
|
ENSP00000362441.4:p.Glu1463Ala
|
|
ENST00000395603.7:c.4274A>C
|
ENSP00000378967.3:p.Glu1425Ala
|
|
ENST00000480283.5:c.*4016A>C
|
ENSP00000480196.1:n.*4016A>C
|
|
NM_000489.4:c.4388A>C
|
NP_000480.3:p.Glu1463Ala
|
|
NM_138270.3:c.4274A>C
|
NP_612114.2:p.Glu1425Ala
|
|
XM_005262153.3:c.4385A>C
|
XP_005262210.2:p.Glu1462Ala
|
|
XM_005262154.3:c.4301A>C
|
XP_005262211.2:p.Glu1434Ala
|
|
XM_005262155.3:c.4271A>C
|
XP_005262212.2:p.Glu1424Ala
|
|
XM_005262156.3:c.4223A>C
|
XP_005262213.2:p.Glu1408Ala
|
|
XM_005262157.3:c.4184A>C
|
XP_005262214.2:p.Glu1395Ala
|
|
XM_006724666.2:c.4271A>C
|
XP_006724729.1:p.Glu1424Ala
|
|
XM_006724667.2:c.4109A>C
|
XP_006724730.1:p.Glu1370Ala
|
|
XM_006724668.2:c.4388A>C
|
XP_006724731.1:p.Glu1463Ala
|
|
XR_938400.1:n.4656A>C
|
|
|
NM_000489.5:c.4388A>C
|
NP_000480.3:p.Glu1463Ala
|
|
XM_005262153.5:c.4385A>C
|
XP_005262210.2:p.Glu1462Ala
|
|
XM_005262154.5:c.4301A>C
|
XP_005262211.2:p.Glu1434Ala
|
|
XM_005262155.4:c.4271A>C
|
XP_005262212.2:p.Glu1424Ala
|
|
XM_005262156.4:c.4223A>C
|
XP_005262213.2:p.Glu1408Ala
|
|
XM_005262157.5:c.4184A>C
|
XP_005262214.2:p.Glu1395Ala
|
|
XM_006724666.4:c.4271A>C
|
XP_006724729.1:p.Glu1424Ala
|
|
XM_006724667.3:c.4109A>C
|
XP_006724730.1:p.Glu1370Ala
|
|
XM_006724668.3:c.4388A>C
|
XP_006724731.1:p.Glu1463Ala
|
|
XM_017029601.2:c.4298A>C
|
XP_016885090.1:p.Glu1433Ala
|
|
XM_017029602.1:c.4268A>C
|
XP_016885091.1:p.Glu1423Ala
|
|
XM_017029603.1:c.4220A>C
|
XP_016885092.1:p.Glu1407Ala
|
|
XM_017029604.2:c.4187A>C
|
XP_016885093.1:p.Glu1396Ala
|
|
XM_017029605.1:c.4184A>C
|
XP_016885094.1:p.Glu1395Ala
|
|
XM_017029606.2:c.4157A>C
|
XP_016885095.1:p.Glu1386Ala
|
|
XM_017029607.2:c.4154A>C
|
XP_016885096.1:p.Glu1385Ala
|
|
XM_017029608.2:c.4106A>C
|
XP_016885097.1:p.Glu1369Ala
|
|
XM_017029609.1:c.4070A>C
|
XP_016885098.1:p.Glu1357Ala
|
|
XM_017029610.1:c.4067A>C
|
XP_016885099.1:p.Glu1356Ala
|
|
XM_017029611.1:c.4022A>C
|
XP_016885100.1:p.Glu1341Ala
|
|
XR_001755700.2:n.4613A>C
|
|
|
NM_138270.4:c.4274A>C
|
NP_612114.2:p.Glu1425Ala
|
|
NM_000489.6:c.4388A>C
MANE Select
|
NP_000480.3:p.Glu1463Ala
|
|
NM_138270.5:c.4274A>C
|
NP_612114.2:p.Glu1425Ala
|
|