ENST00000373344.11:c.4383G>A
MANE Select
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ENSP00000362441.4:p.Glu1461=
|
|
ENST00000373344.9:c.4383G>A
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ENSP00000362441.4:p.Glu1461=
|
|
ENST00000395603.7:c.4269G>A
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ENSP00000378967.3:p.Glu1423=
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|
ENST00000480283.5:c.*4011G>A
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ENSP00000480196.1:n.*4011G>A
|
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NM_000489.4:c.4383G>A
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NP_000480.3:p.Glu1461=
|
|
NM_138270.3:c.4269G>A
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NP_612114.2:p.Glu1423=
|
|
XM_005262153.3:c.4380G>A
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XP_005262210.2:p.Glu1460=
|
|
XM_005262154.3:c.4296G>A
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XP_005262211.2:p.Glu1432=
|
|
XM_005262155.3:c.4266G>A
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XP_005262212.2:p.Glu1422=
|
|
XM_005262156.3:c.4218G>A
|
XP_005262213.2:p.Glu1406=
|
|
XM_005262157.3:c.4179G>A
|
XP_005262214.2:p.Glu1393=
|
|
XM_006724666.2:c.4266G>A
|
XP_006724729.1:p.Glu1422=
|
|
XM_006724667.2:c.4104G>A
|
XP_006724730.1:p.Glu1368=
|
|
XM_006724668.2:c.4383G>A
|
XP_006724731.1:p.Glu1461=
|
|
XR_938400.1:n.4651G>A
|
|
|
NM_000489.5:c.4383G>A
|
NP_000480.3:p.Glu1461=
|
|
XM_005262153.5:c.4380G>A
|
XP_005262210.2:p.Glu1460=
|
|
XM_005262154.5:c.4296G>A
|
XP_005262211.2:p.Glu1432=
|
|
XM_005262155.4:c.4266G>A
|
XP_005262212.2:p.Glu1422=
|
|
XM_005262156.4:c.4218G>A
|
XP_005262213.2:p.Glu1406=
|
|
XM_005262157.5:c.4179G>A
|
XP_005262214.2:p.Glu1393=
|
|
XM_006724666.4:c.4266G>A
|
XP_006724729.1:p.Glu1422=
|
|
XM_006724667.3:c.4104G>A
|
XP_006724730.1:p.Glu1368=
|
|
XM_006724668.3:c.4383G>A
|
XP_006724731.1:p.Glu1461=
|
|
XM_017029601.2:c.4293G>A
|
XP_016885090.1:p.Glu1431=
|
|
XM_017029602.1:c.4263G>A
|
XP_016885091.1:p.Glu1421=
|
|
XM_017029603.1:c.4215G>A
|
XP_016885092.1:p.Glu1405=
|
|
XM_017029604.2:c.4182G>A
|
XP_016885093.1:p.Glu1394=
|
|
XM_017029605.1:c.4179G>A
|
XP_016885094.1:p.Glu1393=
|
|
XM_017029606.2:c.4152G>A
|
XP_016885095.1:p.Glu1384=
|
|
XM_017029607.2:c.4149G>A
|
XP_016885096.1:p.Glu1383=
|
|
XM_017029608.2:c.4101G>A
|
XP_016885097.1:p.Glu1367=
|
|
XM_017029609.1:c.4065G>A
|
XP_016885098.1:p.Glu1355=
|
|
XM_017029610.1:c.4062G>A
|
XP_016885099.1:p.Glu1354=
|
|
XM_017029611.1:c.4017G>A
|
XP_016885100.1:p.Glu1339=
|
|
XR_001755700.2:n.4608G>A
|
|
|
NM_138270.4:c.4269G>A
|
NP_612114.2:p.Glu1423=
|
|
NM_000489.6:c.4383G>A
MANE Select
|
NP_000480.3:p.Glu1461=
|
|
NM_138270.5:c.4269G>A
|
NP_612114.2:p.Glu1423=
|
|