ENST00000373344.11:c.4482A>T
MANE Select
|
ENSP00000362441.4:p.Gln1494His
|
|
ENST00000373344.9:c.4482A>T
|
ENSP00000362441.4:p.Gln1494His
|
|
ENST00000395603.7:c.4368A>T
|
ENSP00000378967.3:p.Gln1456His
|
|
ENST00000480283.5:c.*4110A>T
|
ENSP00000480196.1:n.*4110A>T
|
|
ENST00000623242.3:c.88A>T
|
|
|
NM_000489.4:c.4482A>T
|
NP_000480.3:p.Gln1494His
|
|
NM_138270.3:c.4368A>T
|
NP_612114.2:p.Gln1456His
|
|
XM_005262153.3:c.4479A>T
|
XP_005262210.2:p.Gln1493His
|
|
XM_005262154.3:c.4395A>T
|
XP_005262211.2:p.Gln1465His
|
|
XM_005262155.3:c.4365A>T
|
XP_005262212.2:p.Gln1455His
|
|
XM_005262156.3:c.4317A>T
|
XP_005262213.2:p.Gln1439His
|
|
XM_005262157.3:c.4278A>T
|
XP_005262214.2:p.Gln1426His
|
|
XM_006724666.2:c.4365A>T
|
XP_006724729.1:p.Gln1455His
|
|
XM_006724667.2:c.4203A>T
|
XP_006724730.1:p.Gln1401His
|
|
XM_006724668.2:c.4482A>T
|
XP_006724731.1:p.Gln1494His
|
|
XR_938400.1:n.4750A>T
|
|
|
NM_000489.5:c.4482A>T
|
NP_000480.3:p.Gln1494His
|
|
XM_005262153.5:c.4479A>T
|
XP_005262210.2:p.Gln1493His
|
|
XM_005262154.5:c.4395A>T
|
XP_005262211.2:p.Gln1465His
|
|
XM_005262155.4:c.4365A>T
|
XP_005262212.2:p.Gln1455His
|
|
XM_005262156.4:c.4317A>T
|
XP_005262213.2:p.Gln1439His
|
|
XM_005262157.5:c.4278A>T
|
XP_005262214.2:p.Gln1426His
|
|
XM_006724666.4:c.4365A>T
|
XP_006724729.1:p.Gln1455His
|
|
XM_006724667.3:c.4203A>T
|
XP_006724730.1:p.Gln1401His
|
|
XM_006724668.3:c.4482A>T
|
XP_006724731.1:p.Gln1494His
|
|
XM_017029601.2:c.4392A>T
|
XP_016885090.1:p.Gln1464His
|
|
XM_017029602.1:c.4362A>T
|
XP_016885091.1:p.Gln1454His
|
|
XM_017029603.1:c.4314A>T
|
XP_016885092.1:p.Gln1438His
|
|
XM_017029604.2:c.4281A>T
|
XP_016885093.1:p.Gln1427His
|
|
XM_017029605.1:c.4278A>T
|
XP_016885094.1:p.Gln1426His
|
|
XM_017029606.2:c.4251A>T
|
XP_016885095.1:p.Gln1417His
|
|
XM_017029607.2:c.4248A>T
|
XP_016885096.1:p.Gln1416His
|
|
XM_017029608.2:c.4200A>T
|
XP_016885097.1:p.Gln1400His
|
|
XM_017029609.1:c.4164A>T
|
XP_016885098.1:p.Gln1388His
|
|
XM_017029610.1:c.4161A>T
|
XP_016885099.1:p.Gln1387His
|
|
XM_017029611.1:c.4116A>T
|
XP_016885100.1:p.Gln1372His
|
|
XR_001755700.2:n.4707A>T
|
|
|
NM_138270.4:c.4368A>T
|
NP_612114.2:p.Gln1456His
|
|
NM_000489.6:c.4482A>T
MANE Select
|
NP_000480.3:p.Gln1494His
|
|
NM_138270.5:c.4368A>T
|
NP_612114.2:p.Gln1456His
|
|