ENST00000373344.11:c.2066A>G
MANE Select
|
ENSP00000362441.4:p.Gln689Arg
|
|
ENST00000373344.9:c.2066A>G
|
ENSP00000362441.4:p.Gln689Arg
|
|
ENST00000395603.7:c.1952A>G
|
ENSP00000378967.3:p.Gln651Arg
|
|
ENST00000480283.5:c.*1694A>G
|
ENSP00000480196.1:n.*1694A>G
|
|
ENST00000624032.3:c.1979A>G
|
ENSP00000485253.1:p.Gln660Arg
|
|
ENST00000624166.3:c.1862A>G
|
ENSP00000485103.1:p.Gln621Arg
|
|
NM_000489.4:c.2066A>G
|
NP_000480.3:p.Gln689Arg
|
|
NM_138270.3:c.1952A>G
|
NP_612114.2:p.Gln651Arg
|
|
XM_005262153.3:c.2063A>G
|
XP_005262210.2:p.Gln688Arg
|
|
XM_005262154.3:c.1979A>G
|
XP_005262211.2:p.Gln660Arg
|
|
XM_005262155.3:c.1949A>G
|
XP_005262212.2:p.Gln650Arg
|
|
XM_005262156.3:c.1901A>G
|
XP_005262213.2:p.Gln634Arg
|
|
XM_005262157.3:c.1862A>G
|
XP_005262214.2:p.Gln621Arg
|
|
XM_006724666.2:c.1949A>G
|
XP_006724729.1:p.Gln650Arg
|
|
XM_006724667.2:c.1787A>G
|
XP_006724730.1:p.Gln596Arg
|
|
XM_006724668.2:c.2066A>G
|
XP_006724731.1:p.Gln689Arg
|
|
XR_938400.1:n.2334A>G
|
|
|
NM_000489.5:c.2066A>G
|
NP_000480.3:p.Gln689Arg
|
|
XM_005262153.5:c.2063A>G
|
XP_005262210.2:p.Gln688Arg
|
|
XM_005262154.5:c.1979A>G
|
XP_005262211.2:p.Gln660Arg
|
|
XM_005262155.4:c.1949A>G
|
XP_005262212.2:p.Gln650Arg
|
|
XM_005262156.4:c.1901A>G
|
XP_005262213.2:p.Gln634Arg
|
|
XM_005262157.5:c.1862A>G
|
XP_005262214.2:p.Gln621Arg
|
|
XM_006724666.4:c.1949A>G
|
XP_006724729.1:p.Gln650Arg
|
|
XM_006724667.3:c.1787A>G
|
XP_006724730.1:p.Gln596Arg
|
|
XM_006724668.3:c.2066A>G
|
XP_006724731.1:p.Gln689Arg
|
|
XM_017029601.2:c.1976A>G
|
XP_016885090.1:p.Gln659Arg
|
|
XM_017029602.1:c.1946A>G
|
XP_016885091.1:p.Gln649Arg
|
|
XM_017029603.1:c.1898A>G
|
XP_016885092.1:p.Gln633Arg
|
|
XM_017029604.2:c.1865A>G
|
XP_016885093.1:p.Gln622Arg
|
|
XM_017029605.1:c.1862A>G
|
XP_016885094.1:p.Gln621Arg
|
|
XM_017029606.2:c.1835A>G
|
XP_016885095.1:p.Gln612Arg
|
|
XM_017029607.2:c.1832A>G
|
XP_016885096.1:p.Gln611Arg
|
|
XM_017029608.2:c.1784A>G
|
XP_016885097.1:p.Gln595Arg
|
|
XM_017029609.1:c.1748A>G
|
XP_016885098.1:p.Gln583Arg
|
|
XM_017029610.1:c.1745A>G
|
XP_016885099.1:p.Gln582Arg
|
|
XM_017029611.1:c.1700A>G
|
XP_016885100.1:p.Gln567Arg
|
|
XR_001755700.2:n.2291A>G
|
|
|
NM_138270.4:c.1952A>G
|
NP_612114.2:p.Gln651Arg
|
|
NM_000489.6:c.2066A>G
MANE Select
|
NP_000480.3:p.Gln689Arg
|
|
NM_138270.5:c.1952A>G
|
NP_612114.2:p.Gln651Arg
|
|