ENST00000373344.11:c.7464A>G
MANE Select
|
ENSP00000362441.4:p.Gln2488=
|
|
ENST00000675732.1:c.2562A>G
|
ENSP00000502598.1:p.Gln854=
|
|
ENST00000373344.9:c.7464A>G
|
ENSP00000362441.4:p.Gln2488=
|
|
ENST00000395603.7:c.7350A>G
|
ENSP00000378967.3:p.Gln2450=
|
|
ENST00000480283.5:c.*7092A>G
|
ENSP00000480196.1:n.*7092A>G
|
|
ENST00000623706.3:n.5784A>G
|
|
|
NM_000489.4:c.7464A>G
|
NP_000480.3:p.Gln2488=
|
|
NM_138270.3:c.7350A>G
|
NP_612114.2:p.Gln2450=
|
|
XM_005262153.3:c.7461A>G
|
XP_005262210.2:p.Gln2487=
|
|
XM_005262154.3:c.7377A>G
|
XP_005262211.2:p.Gln2459=
|
|
XM_005262155.3:c.7347A>G
|
XP_005262212.2:p.Gln2449=
|
|
XM_005262156.3:c.7299A>G
|
XP_005262213.2:p.Gln2433=
|
|
XM_005262157.3:c.7260A>G
|
XP_005262214.2:p.Gln2420=
|
|
XM_006724666.2:c.7347A>G
|
XP_006724729.1:p.Gln2449=
|
|
XM_006724667.2:c.7185A>G
|
XP_006724730.1:p.Gln2395=
|
|
XR_938400.1:n.9056A>G
|
|
|
NM_000489.5:c.7464A>G
|
NP_000480.3:p.Gln2488=
|
|
XM_005262153.5:c.7461A>G
|
XP_005262210.2:p.Gln2487=
|
|
XM_005262154.5:c.7377A>G
|
XP_005262211.2:p.Gln2459=
|
|
XM_005262155.4:c.7347A>G
|
XP_005262212.2:p.Gln2449=
|
|
XM_005262156.4:c.7299A>G
|
XP_005262213.2:p.Gln2433=
|
|
XM_005262157.5:c.7260A>G
|
XP_005262214.2:p.Gln2420=
|
|
XM_006724666.4:c.7347A>G
|
XP_006724729.1:p.Gln2449=
|
|
XM_006724667.3:c.7185A>G
|
XP_006724730.1:p.Gln2395=
|
|
XM_017029601.2:c.7374A>G
|
XP_016885090.1:p.Gln2458=
|
|
XM_017029602.1:c.7344A>G
|
XP_016885091.1:p.Gln2448=
|
|
XM_017029603.1:c.7296A>G
|
XP_016885092.1:p.Gln2432=
|
|
XM_017029604.2:c.7263A>G
|
XP_016885093.1:p.Gln2421=
|
|
XM_017029605.1:c.7260A>G
|
XP_016885094.1:p.Gln2420=
|
|
XM_017029606.2:c.7233A>G
|
XP_016885095.1:p.Gln2411=
|
|
XM_017029607.2:c.7230A>G
|
XP_016885096.1:p.Gln2410=
|
|
XM_017029608.2:c.7182A>G
|
XP_016885097.1:p.Gln2394=
|
|
XM_017029609.1:c.7146A>G
|
XP_016885098.1:p.Gln2382=
|
|
XM_017029610.1:c.7143A>G
|
XP_016885099.1:p.Gln2381=
|
|
XM_017029611.1:c.7098A>G
|
XP_016885100.1:p.Gln2366=
|
|
XR_001755700.2:n.7763A>G
|
|
|
NM_138270.4:c.7350A>G
|
NP_612114.2:p.Gln2450=
|
|
NM_000489.6:c.7464A>G
MANE Select
|
NP_000480.3:p.Gln2488=
|
|
NM_138270.5:c.7350A>G
|
NP_612114.2:p.Gln2450=
|
|