ENST00000373344.11:c.4406A>T
MANE Select
|
ENSP00000362441.4:p.Asp1469Val
|
|
ENST00000373344.9:c.4406A>T
|
ENSP00000362441.4:p.Asp1469Val
|
|
ENST00000395603.7:c.4292A>T
|
ENSP00000378967.3:p.Asp1431Val
|
|
ENST00000480283.5:c.*4034A>T
|
ENSP00000480196.1:n.*4034A>T
|
|
ENST00000623242.3:c.12A>T
|
|
|
NM_000489.4:c.4406A>T
|
NP_000480.3:p.Asp1469Val
|
|
NM_138270.3:c.4292A>T
|
NP_612114.2:p.Asp1431Val
|
|
XM_005262153.3:c.4403A>T
|
XP_005262210.2:p.Asp1468Val
|
|
XM_005262154.3:c.4319A>T
|
XP_005262211.2:p.Asp1440Val
|
|
XM_005262155.3:c.4289A>T
|
XP_005262212.2:p.Asp1430Val
|
|
XM_005262156.3:c.4241A>T
|
XP_005262213.2:p.Asp1414Val
|
|
XM_005262157.3:c.4202A>T
|
XP_005262214.2:p.Asp1401Val
|
|
XM_006724666.2:c.4289A>T
|
XP_006724729.1:p.Asp1430Val
|
|
XM_006724667.2:c.4127A>T
|
XP_006724730.1:p.Asp1376Val
|
|
XM_006724668.2:c.4406A>T
|
XP_006724731.1:p.Asp1469Val
|
|
XR_938400.1:n.4674A>T
|
|
|
NM_000489.5:c.4406A>T
|
NP_000480.3:p.Asp1469Val
|
|
XM_005262153.5:c.4403A>T
|
XP_005262210.2:p.Asp1468Val
|
|
XM_005262154.5:c.4319A>T
|
XP_005262211.2:p.Asp1440Val
|
|
XM_005262155.4:c.4289A>T
|
XP_005262212.2:p.Asp1430Val
|
|
XM_005262156.4:c.4241A>T
|
XP_005262213.2:p.Asp1414Val
|
|
XM_005262157.5:c.4202A>T
|
XP_005262214.2:p.Asp1401Val
|
|
XM_006724666.4:c.4289A>T
|
XP_006724729.1:p.Asp1430Val
|
|
XM_006724667.3:c.4127A>T
|
XP_006724730.1:p.Asp1376Val
|
|
XM_006724668.3:c.4406A>T
|
XP_006724731.1:p.Asp1469Val
|
|
XM_017029601.2:c.4316A>T
|
XP_016885090.1:p.Asp1439Val
|
|
XM_017029602.1:c.4286A>T
|
XP_016885091.1:p.Asp1429Val
|
|
XM_017029603.1:c.4238A>T
|
XP_016885092.1:p.Asp1413Val
|
|
XM_017029604.2:c.4205A>T
|
XP_016885093.1:p.Asp1402Val
|
|
XM_017029605.1:c.4202A>T
|
XP_016885094.1:p.Asp1401Val
|
|
XM_017029606.2:c.4175A>T
|
XP_016885095.1:p.Asp1392Val
|
|
XM_017029607.2:c.4172A>T
|
XP_016885096.1:p.Asp1391Val
|
|
XM_017029608.2:c.4124A>T
|
XP_016885097.1:p.Asp1375Val
|
|
XM_017029609.1:c.4088A>T
|
XP_016885098.1:p.Asp1363Val
|
|
XM_017029610.1:c.4085A>T
|
XP_016885099.1:p.Asp1362Val
|
|
XM_017029611.1:c.4040A>T
|
XP_016885100.1:p.Asp1347Val
|
|
XR_001755700.2:n.4631A>T
|
|
|
NM_138270.4:c.4292A>T
|
NP_612114.2:p.Asp1431Val
|
|
NM_000489.6:c.4406A>T
MANE Select
|
NP_000480.3:p.Asp1469Val
|
|
NM_138270.5:c.4292A>T
|
NP_612114.2:p.Asp1431Val
|
|