ENST00000373344.11:c.4354G>T
MANE Select
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ENSP00000362441.4:p.Glu1452Ter
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ENST00000373344.9:c.4354G>T
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ENSP00000362441.4:p.Glu1452Ter
|
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ENST00000395603.7:c.4240G>T
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ENSP00000378967.3:p.Glu1414Ter
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ENST00000480283.5:c.*3982G>T
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ENSP00000480196.1:n.*3982G>T
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NM_000489.4:c.4354G>T
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NP_000480.3:p.Glu1452Ter
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|
NM_138270.3:c.4240G>T
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NP_612114.2:p.Glu1414Ter
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|
XM_005262153.3:c.4351G>T
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XP_005262210.2:p.Glu1451Ter
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XM_005262154.3:c.4267G>T
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XP_005262211.2:p.Glu1423Ter
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XM_005262155.3:c.4237G>T
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XP_005262212.2:p.Glu1413Ter
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|
XM_005262156.3:c.4189G>T
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XP_005262213.2:p.Glu1397Ter
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|
XM_005262157.3:c.4150G>T
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XP_005262214.2:p.Glu1384Ter
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|
XM_006724666.2:c.4237G>T
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XP_006724729.1:p.Glu1413Ter
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|
XM_006724667.2:c.4075G>T
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XP_006724730.1:p.Glu1359Ter
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|
XM_006724668.2:c.4354G>T
|
XP_006724731.1:p.Glu1452Ter
|
|
XR_938400.1:n.4622G>T
|
|
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NM_000489.5:c.4354G>T
|
NP_000480.3:p.Glu1452Ter
|
|
XM_005262153.5:c.4351G>T
|
XP_005262210.2:p.Glu1451Ter
|
|
XM_005262154.5:c.4267G>T
|
XP_005262211.2:p.Glu1423Ter
|
|
XM_005262155.4:c.4237G>T
|
XP_005262212.2:p.Glu1413Ter
|
|
XM_005262156.4:c.4189G>T
|
XP_005262213.2:p.Glu1397Ter
|
|
XM_005262157.5:c.4150G>T
|
XP_005262214.2:p.Glu1384Ter
|
|
XM_006724666.4:c.4237G>T
|
XP_006724729.1:p.Glu1413Ter
|
|
XM_006724667.3:c.4075G>T
|
XP_006724730.1:p.Glu1359Ter
|
|
XM_006724668.3:c.4354G>T
|
XP_006724731.1:p.Glu1452Ter
|
|
XM_017029601.2:c.4264G>T
|
XP_016885090.1:p.Glu1422Ter
|
|
XM_017029602.1:c.4234G>T
|
XP_016885091.1:p.Glu1412Ter
|
|
XM_017029603.1:c.4186G>T
|
XP_016885092.1:p.Glu1396Ter
|
|
XM_017029604.2:c.4153G>T
|
XP_016885093.1:p.Glu1385Ter
|
|
XM_017029605.1:c.4150G>T
|
XP_016885094.1:p.Glu1384Ter
|
|
XM_017029606.2:c.4123G>T
|
XP_016885095.1:p.Glu1375Ter
|
|
XM_017029607.2:c.4120G>T
|
XP_016885096.1:p.Glu1374Ter
|
|
XM_017029608.2:c.4072G>T
|
XP_016885097.1:p.Glu1358Ter
|
|
XM_017029609.1:c.4036G>T
|
XP_016885098.1:p.Glu1346Ter
|
|
XM_017029610.1:c.4033G>T
|
XP_016885099.1:p.Glu1345Ter
|
|
XM_017029611.1:c.3988G>T
|
XP_016885100.1:p.Glu1330Ter
|
|
XR_001755700.2:n.4579G>T
|
|
|
NM_138270.4:c.4240G>T
|
NP_612114.2:p.Glu1414Ter
|
|
NM_000489.6:c.4354G>T
MANE Select
|
NP_000480.3:p.Glu1452Ter
|
|
NM_138270.5:c.4240G>T
|
NP_612114.2:p.Glu1414Ter
|
|