ENST00000373344.11:c.4330G>T
MANE Select
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ENSP00000362441.4:p.Glu1444Ter
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ENST00000373344.9:c.4330G>T
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ENSP00000362441.4:p.Glu1444Ter
|
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ENST00000395603.7:c.4216G>T
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ENSP00000378967.3:p.Glu1406Ter
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ENST00000480283.5:c.*3958G>T
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ENSP00000480196.1:n.*3958G>T
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NM_000489.4:c.4330G>T
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NP_000480.3:p.Glu1444Ter
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|
NM_138270.3:c.4216G>T
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NP_612114.2:p.Glu1406Ter
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|
XM_005262153.3:c.4327G>T
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XP_005262210.2:p.Glu1443Ter
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XM_005262154.3:c.4243G>T
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XP_005262211.2:p.Glu1415Ter
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|
XM_005262155.3:c.4213G>T
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XP_005262212.2:p.Glu1405Ter
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|
XM_005262156.3:c.4165G>T
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XP_005262213.2:p.Glu1389Ter
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|
XM_005262157.3:c.4126G>T
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XP_005262214.2:p.Glu1376Ter
|
|
XM_006724666.2:c.4213G>T
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XP_006724729.1:p.Glu1405Ter
|
|
XM_006724667.2:c.4051G>T
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XP_006724730.1:p.Glu1351Ter
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|
XM_006724668.2:c.4330G>T
|
XP_006724731.1:p.Glu1444Ter
|
|
XR_938400.1:n.4598G>T
|
|
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NM_000489.5:c.4330G>T
|
NP_000480.3:p.Glu1444Ter
|
|
XM_005262153.5:c.4327G>T
|
XP_005262210.2:p.Glu1443Ter
|
|
XM_005262154.5:c.4243G>T
|
XP_005262211.2:p.Glu1415Ter
|
|
XM_005262155.4:c.4213G>T
|
XP_005262212.2:p.Glu1405Ter
|
|
XM_005262156.4:c.4165G>T
|
XP_005262213.2:p.Glu1389Ter
|
|
XM_005262157.5:c.4126G>T
|
XP_005262214.2:p.Glu1376Ter
|
|
XM_006724666.4:c.4213G>T
|
XP_006724729.1:p.Glu1405Ter
|
|
XM_006724667.3:c.4051G>T
|
XP_006724730.1:p.Glu1351Ter
|
|
XM_006724668.3:c.4330G>T
|
XP_006724731.1:p.Glu1444Ter
|
|
XM_017029601.2:c.4240G>T
|
XP_016885090.1:p.Glu1414Ter
|
|
XM_017029602.1:c.4210G>T
|
XP_016885091.1:p.Glu1404Ter
|
|
XM_017029603.1:c.4162G>T
|
XP_016885092.1:p.Glu1388Ter
|
|
XM_017029604.2:c.4129G>T
|
XP_016885093.1:p.Glu1377Ter
|
|
XM_017029605.1:c.4126G>T
|
XP_016885094.1:p.Glu1376Ter
|
|
XM_017029606.2:c.4099G>T
|
XP_016885095.1:p.Glu1367Ter
|
|
XM_017029607.2:c.4096G>T
|
XP_016885096.1:p.Glu1366Ter
|
|
XM_017029608.2:c.4048G>T
|
XP_016885097.1:p.Glu1350Ter
|
|
XM_017029609.1:c.4012G>T
|
XP_016885098.1:p.Glu1338Ter
|
|
XM_017029610.1:c.4009G>T
|
XP_016885099.1:p.Glu1337Ter
|
|
XM_017029611.1:c.3964G>T
|
XP_016885100.1:p.Glu1322Ter
|
|
XR_001755700.2:n.4555G>T
|
|
|
NM_138270.4:c.4216G>T
|
NP_612114.2:p.Glu1406Ter
|
|
NM_000489.6:c.4330G>T
MANE Select
|
NP_000480.3:p.Glu1444Ter
|
|
NM_138270.5:c.4216G>T
|
NP_612114.2:p.Glu1406Ter
|
|