ENST00000373344.11:c.4353G>T
MANE Select
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ENSP00000362441.4:p.Glu1451Asp
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ENST00000373344.9:c.4353G>T
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ENSP00000362441.4:p.Glu1451Asp
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|
ENST00000395603.7:c.4239G>T
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ENSP00000378967.3:p.Glu1413Asp
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ENST00000480283.5:c.*3981G>T
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ENSP00000480196.1:n.*3981G>T
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NM_000489.4:c.4353G>T
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NP_000480.3:p.Glu1451Asp
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|
NM_138270.3:c.4239G>T
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NP_612114.2:p.Glu1413Asp
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XM_005262153.3:c.4350G>T
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XP_005262210.2:p.Glu1450Asp
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XM_005262154.3:c.4266G>T
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XP_005262211.2:p.Glu1422Asp
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XM_005262155.3:c.4236G>T
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XP_005262212.2:p.Glu1412Asp
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|
XM_005262156.3:c.4188G>T
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XP_005262213.2:p.Glu1396Asp
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XM_005262157.3:c.4149G>T
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XP_005262214.2:p.Glu1383Asp
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|
XM_006724666.2:c.4236G>T
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XP_006724729.1:p.Glu1412Asp
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|
XM_006724667.2:c.4074G>T
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XP_006724730.1:p.Glu1358Asp
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XM_006724668.2:c.4353G>T
|
XP_006724731.1:p.Glu1451Asp
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XR_938400.1:n.4621G>T
|
|
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NM_000489.5:c.4353G>T
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NP_000480.3:p.Glu1451Asp
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|
XM_005262153.5:c.4350G>T
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XP_005262210.2:p.Glu1450Asp
|
|
XM_005262154.5:c.4266G>T
|
XP_005262211.2:p.Glu1422Asp
|
|
XM_005262155.4:c.4236G>T
|
XP_005262212.2:p.Glu1412Asp
|
|
XM_005262156.4:c.4188G>T
|
XP_005262213.2:p.Glu1396Asp
|
|
XM_005262157.5:c.4149G>T
|
XP_005262214.2:p.Glu1383Asp
|
|
XM_006724666.4:c.4236G>T
|
XP_006724729.1:p.Glu1412Asp
|
|
XM_006724667.3:c.4074G>T
|
XP_006724730.1:p.Glu1358Asp
|
|
XM_006724668.3:c.4353G>T
|
XP_006724731.1:p.Glu1451Asp
|
|
XM_017029601.2:c.4263G>T
|
XP_016885090.1:p.Glu1421Asp
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|
XM_017029602.1:c.4233G>T
|
XP_016885091.1:p.Glu1411Asp
|
|
XM_017029603.1:c.4185G>T
|
XP_016885092.1:p.Glu1395Asp
|
|
XM_017029604.2:c.4152G>T
|
XP_016885093.1:p.Glu1384Asp
|
|
XM_017029605.1:c.4149G>T
|
XP_016885094.1:p.Glu1383Asp
|
|
XM_017029606.2:c.4122G>T
|
XP_016885095.1:p.Glu1374Asp
|
|
XM_017029607.2:c.4119G>T
|
XP_016885096.1:p.Glu1373Asp
|
|
XM_017029608.2:c.4071G>T
|
XP_016885097.1:p.Glu1357Asp
|
|
XM_017029609.1:c.4035G>T
|
XP_016885098.1:p.Glu1345Asp
|
|
XM_017029610.1:c.4032G>T
|
XP_016885099.1:p.Glu1344Asp
|
|
XM_017029611.1:c.3987G>T
|
XP_016885100.1:p.Glu1329Asp
|
|
XR_001755700.2:n.4578G>T
|
|
|
NM_138270.4:c.4239G>T
|
NP_612114.2:p.Glu1413Asp
|
|
NM_000489.6:c.4353G>T
MANE Select
|
NP_000480.3:p.Glu1451Asp
|
|
NM_138270.5:c.4239G>T
|
NP_612114.2:p.Glu1413Asp
|
|