ENST00000373344.11:c.4399A>C
MANE Select
|
ENSP00000362441.4:p.Asn1467His
|
|
ENST00000373344.9:c.4399A>C
|
ENSP00000362441.4:p.Asn1467His
|
|
ENST00000395603.7:c.4285A>C
|
ENSP00000378967.3:p.Asn1429His
|
|
ENST00000480283.5:c.*4027A>C
|
ENSP00000480196.1:n.*4027A>C
|
|
ENST00000623242.3:c.5A>C
|
|
|
NM_000489.4:c.4399A>C
|
NP_000480.3:p.Asn1467His
|
|
NM_138270.3:c.4285A>C
|
NP_612114.2:p.Asn1429His
|
|
XM_005262153.3:c.4396A>C
|
XP_005262210.2:p.Asn1466His
|
|
XM_005262154.3:c.4312A>C
|
XP_005262211.2:p.Asn1438His
|
|
XM_005262155.3:c.4282A>C
|
XP_005262212.2:p.Asn1428His
|
|
XM_005262156.3:c.4234A>C
|
XP_005262213.2:p.Asn1412His
|
|
XM_005262157.3:c.4195A>C
|
XP_005262214.2:p.Asn1399His
|
|
XM_006724666.2:c.4282A>C
|
XP_006724729.1:p.Asn1428His
|
|
XM_006724667.2:c.4120A>C
|
XP_006724730.1:p.Asn1374His
|
|
XM_006724668.2:c.4399A>C
|
XP_006724731.1:p.Asn1467His
|
|
XR_938400.1:n.4667A>C
|
|
|
NM_000489.5:c.4399A>C
|
NP_000480.3:p.Asn1467His
|
|
XM_005262153.5:c.4396A>C
|
XP_005262210.2:p.Asn1466His
|
|
XM_005262154.5:c.4312A>C
|
XP_005262211.2:p.Asn1438His
|
|
XM_005262155.4:c.4282A>C
|
XP_005262212.2:p.Asn1428His
|
|
XM_005262156.4:c.4234A>C
|
XP_005262213.2:p.Asn1412His
|
|
XM_005262157.5:c.4195A>C
|
XP_005262214.2:p.Asn1399His
|
|
XM_006724666.4:c.4282A>C
|
XP_006724729.1:p.Asn1428His
|
|
XM_006724667.3:c.4120A>C
|
XP_006724730.1:p.Asn1374His
|
|
XM_006724668.3:c.4399A>C
|
XP_006724731.1:p.Asn1467His
|
|
XM_017029601.2:c.4309A>C
|
XP_016885090.1:p.Asn1437His
|
|
XM_017029602.1:c.4279A>C
|
XP_016885091.1:p.Asn1427His
|
|
XM_017029603.1:c.4231A>C
|
XP_016885092.1:p.Asn1411His
|
|
XM_017029604.2:c.4198A>C
|
XP_016885093.1:p.Asn1400His
|
|
XM_017029605.1:c.4195A>C
|
XP_016885094.1:p.Asn1399His
|
|
XM_017029606.2:c.4168A>C
|
XP_016885095.1:p.Asn1390His
|
|
XM_017029607.2:c.4165A>C
|
XP_016885096.1:p.Asn1389His
|
|
XM_017029608.2:c.4117A>C
|
XP_016885097.1:p.Asn1373His
|
|
XM_017029609.1:c.4081A>C
|
XP_016885098.1:p.Asn1361His
|
|
XM_017029610.1:c.4078A>C
|
XP_016885099.1:p.Asn1360His
|
|
XM_017029611.1:c.4033A>C
|
XP_016885100.1:p.Asn1345His
|
|
XR_001755700.2:n.4624A>C
|
|
|
NM_138270.4:c.4285A>C
|
NP_612114.2:p.Asn1429His
|
|
NM_000489.6:c.4399A>C
MANE Select
|
NP_000480.3:p.Asn1467His
|
|
NM_138270.5:c.4285A>C
|
NP_612114.2:p.Asn1429His
|
|