ENST00000373344.11:c.4396G>T
MANE Select
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ENSP00000362441.4:p.Glu1466Ter
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ENST00000373344.9:c.4396G>T
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ENSP00000362441.4:p.Glu1466Ter
|
|
ENST00000395603.7:c.4282G>T
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ENSP00000378967.3:p.Glu1428Ter
|
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ENST00000480283.5:c.*4024G>T
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ENSP00000480196.1:n.*4024G>T
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ENST00000623242.3:c.2G>T
|
|
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NM_000489.4:c.4396G>T
|
NP_000480.3:p.Glu1466Ter
|
|
NM_138270.3:c.4282G>T
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NP_612114.2:p.Glu1428Ter
|
|
XM_005262153.3:c.4393G>T
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XP_005262210.2:p.Glu1465Ter
|
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XM_005262154.3:c.4309G>T
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XP_005262211.2:p.Glu1437Ter
|
|
XM_005262155.3:c.4279G>T
|
XP_005262212.2:p.Glu1427Ter
|
|
XM_005262156.3:c.4231G>T
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XP_005262213.2:p.Glu1411Ter
|
|
XM_005262157.3:c.4192G>T
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XP_005262214.2:p.Glu1398Ter
|
|
XM_006724666.2:c.4279G>T
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XP_006724729.1:p.Glu1427Ter
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|
XM_006724667.2:c.4117G>T
|
XP_006724730.1:p.Glu1373Ter
|
|
XM_006724668.2:c.4396G>T
|
XP_006724731.1:p.Glu1466Ter
|
|
XR_938400.1:n.4664G>T
|
|
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NM_000489.5:c.4396G>T
|
NP_000480.3:p.Glu1466Ter
|
|
XM_005262153.5:c.4393G>T
|
XP_005262210.2:p.Glu1465Ter
|
|
XM_005262154.5:c.4309G>T
|
XP_005262211.2:p.Glu1437Ter
|
|
XM_005262155.4:c.4279G>T
|
XP_005262212.2:p.Glu1427Ter
|
|
XM_005262156.4:c.4231G>T
|
XP_005262213.2:p.Glu1411Ter
|
|
XM_005262157.5:c.4192G>T
|
XP_005262214.2:p.Glu1398Ter
|
|
XM_006724666.4:c.4279G>T
|
XP_006724729.1:p.Glu1427Ter
|
|
XM_006724667.3:c.4117G>T
|
XP_006724730.1:p.Glu1373Ter
|
|
XM_006724668.3:c.4396G>T
|
XP_006724731.1:p.Glu1466Ter
|
|
XM_017029601.2:c.4306G>T
|
XP_016885090.1:p.Glu1436Ter
|
|
XM_017029602.1:c.4276G>T
|
XP_016885091.1:p.Glu1426Ter
|
|
XM_017029603.1:c.4228G>T
|
XP_016885092.1:p.Glu1410Ter
|
|
XM_017029604.2:c.4195G>T
|
XP_016885093.1:p.Glu1399Ter
|
|
XM_017029605.1:c.4192G>T
|
XP_016885094.1:p.Glu1398Ter
|
|
XM_017029606.2:c.4165G>T
|
XP_016885095.1:p.Glu1389Ter
|
|
XM_017029607.2:c.4162G>T
|
XP_016885096.1:p.Glu1388Ter
|
|
XM_017029608.2:c.4114G>T
|
XP_016885097.1:p.Glu1372Ter
|
|
XM_017029609.1:c.4078G>T
|
XP_016885098.1:p.Glu1360Ter
|
|
XM_017029610.1:c.4075G>T
|
XP_016885099.1:p.Glu1359Ter
|
|
XM_017029611.1:c.4030G>T
|
XP_016885100.1:p.Glu1344Ter
|
|
XR_001755700.2:n.4621G>T
|
|
|
NM_138270.4:c.4282G>T
|
NP_612114.2:p.Glu1428Ter
|
|
NM_000489.6:c.4396G>T
MANE Select
|
NP_000480.3:p.Glu1466Ter
|
|
NM_138270.5:c.4282G>T
|
NP_612114.2:p.Glu1428Ter
|
|