ENST00000373344.11:c.4404T=
MANE Select
|
ENSP00000362441.4:p.Asp1468=
|
|
ENST00000373344.9:c.4404T=
|
ENSP00000362441.4:p.Asp1468=
|
|
ENST00000395603.7:c.4290T=
|
ENSP00000378967.3:p.Asp1430=
|
|
ENST00000480283.5:c.*4032T=
|
ENSP00000480196.1:n.*4032T=
|
|
ENST00000623242.3:c.10T=
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|
|
NM_000489.4:c.4404T=
|
NP_000480.3:p.Asp1468=
|
|
NM_138270.3:c.4290T=
|
NP_612114.2:p.Asp1430=
|
|
XM_005262153.3:c.4401T=
|
XP_005262210.2:p.Asp1467=
|
|
XM_005262154.3:c.4317T=
|
XP_005262211.2:p.Asp1439=
|
|
XM_005262155.3:c.4287T=
|
XP_005262212.2:p.Asp1429=
|
|
XM_005262156.3:c.4239T=
|
XP_005262213.2:p.Asp1413=
|
|
XM_005262157.3:c.4200T=
|
XP_005262214.2:p.Asp1400=
|
|
XM_006724666.2:c.4287T=
|
XP_006724729.1:p.Asp1429=
|
|
XM_006724667.2:c.4125T=
|
XP_006724730.1:p.Asp1375=
|
|
XM_006724668.2:c.4404T=
|
XP_006724731.1:p.Asp1468=
|
|
XR_938400.1:n.4672T=
|
|
|
NM_000489.5:c.4404T=
|
NP_000480.3:p.Asp1468=
|
|
XM_005262153.5:c.4401T=
|
XP_005262210.2:p.Asp1467=
|
|
XM_005262154.5:c.4317T=
|
XP_005262211.2:p.Asp1439=
|
|
XM_005262155.4:c.4287T=
|
XP_005262212.2:p.Asp1429=
|
|
XM_005262156.4:c.4239T=
|
XP_005262213.2:p.Asp1413=
|
|
XM_005262157.5:c.4200T=
|
XP_005262214.2:p.Asp1400=
|
|
XM_006724666.4:c.4287T=
|
XP_006724729.1:p.Asp1429=
|
|
XM_006724667.3:c.4125T=
|
XP_006724730.1:p.Asp1375=
|
|
XM_006724668.3:c.4404T=
|
XP_006724731.1:p.Asp1468=
|
|
XM_017029601.2:c.4314T=
|
XP_016885090.1:p.Asp1438=
|
|
XM_017029602.1:c.4284T=
|
XP_016885091.1:p.Asp1428=
|
|
XM_017029603.1:c.4236T=
|
XP_016885092.1:p.Asp1412=
|
|
XM_017029604.2:c.4203T=
|
XP_016885093.1:p.Asp1401=
|
|
XM_017029605.1:c.4200T=
|
XP_016885094.1:p.Asp1400=
|
|
XM_017029606.2:c.4173T=
|
XP_016885095.1:p.Asp1391=
|
|
XM_017029607.2:c.4170T=
|
XP_016885096.1:p.Asp1390=
|
|
XM_017029608.2:c.4122T=
|
XP_016885097.1:p.Asp1374=
|
|
XM_017029609.1:c.4086T=
|
XP_016885098.1:p.Asp1362=
|
|
XM_017029610.1:c.4083T=
|
XP_016885099.1:p.Asp1361=
|
|
XM_017029611.1:c.4038T=
|
XP_016885100.1:p.Asp1346=
|
|
XR_001755700.2:n.4629T=
|
|
|
NM_138270.4:c.4290T=
|
NP_612114.2:p.Asp1430=
|
|
NM_000489.6:c.4404T=
MANE Select
|
NP_000480.3:p.Asp1468=
|
|
NM_138270.5:c.4290T=
|
NP_612114.2:p.Asp1430=
|
|