ENST00000373344.11:c.4474G>T
MANE Select
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ENSP00000362441.4:p.Glu1492Ter
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ENST00000373344.9:c.4474G>T
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ENSP00000362441.4:p.Glu1492Ter
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ENST00000395603.7:c.4360G>T
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ENSP00000378967.3:p.Glu1454Ter
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ENST00000480283.5:c.*4102G>T
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ENSP00000480196.1:n.*4102G>T
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ENST00000623242.3:c.80G>T
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|
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NM_000489.4:c.4474G>T
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NP_000480.3:p.Glu1492Ter
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NM_138270.3:c.4360G>T
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NP_612114.2:p.Glu1454Ter
|
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XM_005262153.3:c.4471G>T
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XP_005262210.2:p.Glu1491Ter
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XM_005262154.3:c.4387G>T
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XP_005262211.2:p.Glu1463Ter
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XM_005262155.3:c.4357G>T
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XP_005262212.2:p.Glu1453Ter
|
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XM_005262156.3:c.4309G>T
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XP_005262213.2:p.Glu1437Ter
|
|
XM_005262157.3:c.4270G>T
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XP_005262214.2:p.Glu1424Ter
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XM_006724666.2:c.4357G>T
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XP_006724729.1:p.Glu1453Ter
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XM_006724667.2:c.4195G>T
|
XP_006724730.1:p.Glu1399Ter
|
|
XM_006724668.2:c.4474G>T
|
XP_006724731.1:p.Glu1492Ter
|
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XR_938400.1:n.4742G>T
|
|
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NM_000489.5:c.4474G>T
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NP_000480.3:p.Glu1492Ter
|
|
XM_005262153.5:c.4471G>T
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XP_005262210.2:p.Glu1491Ter
|
|
XM_005262154.5:c.4387G>T
|
XP_005262211.2:p.Glu1463Ter
|
|
XM_005262155.4:c.4357G>T
|
XP_005262212.2:p.Glu1453Ter
|
|
XM_005262156.4:c.4309G>T
|
XP_005262213.2:p.Glu1437Ter
|
|
XM_005262157.5:c.4270G>T
|
XP_005262214.2:p.Glu1424Ter
|
|
XM_006724666.4:c.4357G>T
|
XP_006724729.1:p.Glu1453Ter
|
|
XM_006724667.3:c.4195G>T
|
XP_006724730.1:p.Glu1399Ter
|
|
XM_006724668.3:c.4474G>T
|
XP_006724731.1:p.Glu1492Ter
|
|
XM_017029601.2:c.4384G>T
|
XP_016885090.1:p.Glu1462Ter
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|
XM_017029602.1:c.4354G>T
|
XP_016885091.1:p.Glu1452Ter
|
|
XM_017029603.1:c.4306G>T
|
XP_016885092.1:p.Glu1436Ter
|
|
XM_017029604.2:c.4273G>T
|
XP_016885093.1:p.Glu1425Ter
|
|
XM_017029605.1:c.4270G>T
|
XP_016885094.1:p.Glu1424Ter
|
|
XM_017029606.2:c.4243G>T
|
XP_016885095.1:p.Glu1415Ter
|
|
XM_017029607.2:c.4240G>T
|
XP_016885096.1:p.Glu1414Ter
|
|
XM_017029608.2:c.4192G>T
|
XP_016885097.1:p.Glu1398Ter
|
|
XM_017029609.1:c.4156G>T
|
XP_016885098.1:p.Glu1386Ter
|
|
XM_017029610.1:c.4153G>T
|
XP_016885099.1:p.Glu1385Ter
|
|
XM_017029611.1:c.4108G>T
|
XP_016885100.1:p.Glu1370Ter
|
|
XR_001755700.2:n.4699G>T
|
|
|
NM_138270.4:c.4360G>T
|
NP_612114.2:p.Glu1454Ter
|
|
NM_000489.6:c.4474G>T
MANE Select
|
NP_000480.3:p.Glu1492Ter
|
|
NM_138270.5:c.4360G>T
|
NP_612114.2:p.Glu1454Ter
|
|