|
ENST00000524470.2:c.*1242T>G
|
ENSP00000514307.1:n.*1242T>G
|
|
|
ENST00000525976.6:c.2893T>G
|
ENSP00000434831.2:p.Cys965Gly
|
|
|
ENST00000527481.3:c.2893T>G
|
ENSP00000466340.2:p.Cys965Gly
|
|
|
ENST00000529370.6:n.4269T>G
|
|
|
|
ENST00000529739.2:n.3307T>G
|
|
|
|
ENST00000530829.2:c.*2444T>G
|
ENSP00000436826.2:n.*2444T>G
|
|
|
ENST00000531836.6:c.2893T>G
|
ENSP00000436175.2:p.Cys965Gly
|
|
|
ENST00000533334.2:c.*935T>G
|
ENSP00000432320.2:n.*935T>G
|
|
|
ENST00000534228.2:n.4352T>G
|
|
|
|
ENST00000699354.1:n.995T>G
|
|
|
|
ENST00000699355.1:c.*1998T>G
|
ENSP00000514328.1:n.*1998T>G
|
|
|
ENST00000699356.1:n.3307T>G
|
|
|
|
ENST00000699357.1:n.4352T>G
|
|
|
|
ENST00000699358.1:c.2893T>G
|
ENSP00000514329.1:p.Cys965Gly
|
|
|
ENST00000699359.1:c.99T>G
|
|
|
|
ENST00000699360.1:c.2893T>G
|
ENSP00000514331.1:p.Cys965Gly
|
|
|
ENST00000699368.1:c.97T>G
|
ENSP00000514335.1:p.Cys33Gly
|
|
|
ENST00000525621.6:c.2893T>G
MANE Select
|
ENSP00000431885.1:p.Cys965Gly
|
|
|
ENST00000264818.10:c.2893T>G
|
ENSP00000264818.6:p.Cys965Gly
|
|
|
ENST00000524462.5:c.2338T>G
|
ENSP00000433203.1:p.Cys780Gly
|
|
|
ENST00000525621.5:c.2893T>G
|
ENSP00000431885.1:p.Cys965Gly
|
|
|
ENST00000527481.2:c.189T>G
|
|
|
|
ENST00000529412.1:n.565T>G
|
|
|
|
ENST00000529739.1:c.-434T>G
|
ENSP00000436155.1:n.-434T>G
|
|
|
ENST00000530560.5:c.322T>G
|
ENSP00000465291.1:p.Cys108Gly
|
|
|
ENST00000592137.1:n.47T>G
|
|
|
|
NM_003331.4:c.2893T>G , LRG_121t1:c.2893T>G
|
NP_003322.3:p.Cys965Gly
|
|
|
XM_011528245.1:c.2893T>G
|
XP_011526547.1:p.Cys965Gly
|
|
|
XM_011528246.1:c.2596T>G
|
XP_011526548.1:p.Cys866Gly
|
|
|
XM_011528247.1:c.2596T>G
|
XP_011526549.1:p.Cys866Gly
|
|
|
XM_011528248.1:c.2893T>G
|
XP_011526550.1:p.Cys965Gly
|
|
|
XM_011528249.1:c.1567T>G
|
XP_011526551.1:p.Cys523Gly
|
|
|
XM_011528251.1:c.1150T>G
|
XP_011526553.1:p.Cys384Gly
|
|
|
XM_011528246.3:c.2596T>G
|
XP_011526548.1:p.Cys866Gly
|
|
|
XM_011528249.2:c.1567T>G
|
XP_011526551.1:p.Cys523Gly
|
|
|
XR_001753750.1:n.3050T>G
|
|
|
|
XR_001753751.1:n.3050T>G
|
|
|
|
XR_002958353.1:n.3976T>G
|
|
|
|
NM_003331.5:c.2893T>G
MANE Select
|
NP_003322.3:p.Cys965Gly
|
|
|
NM_001385197.1:c.2893T>G
|
NP_001372126.1:p.Cys965Gly
|
|
|
NM_001385198.1:c.2893T>G
|
NP_001372127.1:p.Cys965Gly
|
|
|
NM_001385199.1:c.2707T>G
|
NP_001372128.1:p.Cys903Gly
|
|
|
NM_001385200.1:c.2890T>G
|
NP_001372129.1:p.Cys964Gly
|
|
|
NM_001385201.1:c.2695T>G
|
NP_001372130.1:p.Cys899Gly
|
|
|
NM_001385202.1:c.2809T>G
|
NP_001372131.1:p.Cys937Gly
|
|
|
NM_001385203.1:c.2974T>G
|
NP_001372132.1:p.Cys992Gly
|
|
|
NM_001385204.1:c.3103T>G
|
NP_001372133.1:p.Cys1035Gly
|
|
|
NM_001385205.1:c.2803T>G
|
NP_001372134.1:p.Cys935Gly
|
|
|
NM_001385206.1:c.2767T>G
|
NP_001372135.1:p.Cys923Gly
|
|
|
NM_001385207.1:c.2875T>G
|
NP_001372136.1:p.Cys959Gly
|
|
