ENST00000373344.11:c.4365G>C
MANE Select
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ENSP00000362441.4:p.Glu1455Asp
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ENST00000373344.9:c.4365G>C
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ENSP00000362441.4:p.Glu1455Asp
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|
ENST00000395603.7:c.4251G>C
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ENSP00000378967.3:p.Glu1417Asp
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|
ENST00000480283.5:c.*3993G>C
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ENSP00000480196.1:n.*3993G>C
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NM_000489.4:c.4365G>C
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NP_000480.3:p.Glu1455Asp
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|
NM_138270.3:c.4251G>C
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NP_612114.2:p.Glu1417Asp
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|
XM_005262153.3:c.4362G>C
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XP_005262210.2:p.Glu1454Asp
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XM_005262154.3:c.4278G>C
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XP_005262211.2:p.Glu1426Asp
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|
XM_005262155.3:c.4248G>C
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XP_005262212.2:p.Glu1416Asp
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|
XM_005262156.3:c.4200G>C
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XP_005262213.2:p.Glu1400Asp
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XM_005262157.3:c.4161G>C
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XP_005262214.2:p.Glu1387Asp
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|
XM_006724666.2:c.4248G>C
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XP_006724729.1:p.Glu1416Asp
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|
XM_006724667.2:c.4086G>C
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XP_006724730.1:p.Glu1362Asp
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XM_006724668.2:c.4365G>C
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XP_006724731.1:p.Glu1455Asp
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XR_938400.1:n.4633G>C
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|
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NM_000489.5:c.4365G>C
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NP_000480.3:p.Glu1455Asp
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|
XM_005262153.5:c.4362G>C
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XP_005262210.2:p.Glu1454Asp
|
|
XM_005262154.5:c.4278G>C
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XP_005262211.2:p.Glu1426Asp
|
|
XM_005262155.4:c.4248G>C
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XP_005262212.2:p.Glu1416Asp
|
|
XM_005262156.4:c.4200G>C
|
XP_005262213.2:p.Glu1400Asp
|
|
XM_005262157.5:c.4161G>C
|
XP_005262214.2:p.Glu1387Asp
|
|
XM_006724666.4:c.4248G>C
|
XP_006724729.1:p.Glu1416Asp
|
|
XM_006724667.3:c.4086G>C
|
XP_006724730.1:p.Glu1362Asp
|
|
XM_006724668.3:c.4365G>C
|
XP_006724731.1:p.Glu1455Asp
|
|
XM_017029601.2:c.4275G>C
|
XP_016885090.1:p.Glu1425Asp
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|
XM_017029602.1:c.4245G>C
|
XP_016885091.1:p.Glu1415Asp
|
|
XM_017029603.1:c.4197G>C
|
XP_016885092.1:p.Glu1399Asp
|
|
XM_017029604.2:c.4164G>C
|
XP_016885093.1:p.Glu1388Asp
|
|
XM_017029605.1:c.4161G>C
|
XP_016885094.1:p.Glu1387Asp
|
|
XM_017029606.2:c.4134G>C
|
XP_016885095.1:p.Glu1378Asp
|
|
XM_017029607.2:c.4131G>C
|
XP_016885096.1:p.Glu1377Asp
|
|
XM_017029608.2:c.4083G>C
|
XP_016885097.1:p.Glu1361Asp
|
|
XM_017029609.1:c.4047G>C
|
XP_016885098.1:p.Glu1349Asp
|
|
XM_017029610.1:c.4044G>C
|
XP_016885099.1:p.Glu1348Asp
|
|
XM_017029611.1:c.3999G>C
|
XP_016885100.1:p.Glu1333Asp
|
|
XR_001755700.2:n.4590G>C
|
|
|
NM_138270.4:c.4251G>C
|
NP_612114.2:p.Glu1417Asp
|
|
NM_000489.6:c.4365G>C
MANE Select
|
NP_000480.3:p.Glu1455Asp
|
|
NM_138270.5:c.4251G>C
|
NP_612114.2:p.Glu1417Asp
|
|