|
ENST00000570382.2:c.404C>T
|
ENSP00000466346.2:p.Ala135Val
|
|
|
ENST00000571691.6:c.340-8C>T
|
ENSP00000461407.2:n.340-8C>T
|
|
|
ENST00000571721.6:c.404C>T
|
ENSP00000460660.2:p.Ala135Val
|
|
|
ENST00000572105.7:c.445C>T
|
ENSP00000462823.1:p.Pro149Ser
|
|
|
ENST00000573283.7:c.404C>T
MANE Select
|
ENSP00000458435.1:p.Ala135Val
|
|
|
ENST00000574671.6:n.804C>T
|
|
|
|
ENST00000575659.6:c.404C>T
|
ENSP00000459119.2:p.Ala135Val
|
|
|
ENST00000575994.6:c.404C>T
|
ENSP00000460464.2:p.Ala135Val
|
|
|
ENST00000576214.3:n.705C>T
|
|
|
|
ENST00000576544.6:c.404C>T
|
ENSP00000461672.1:p.Ala135Val
|
|
|
ENST00000615544.5:c.404C>T
|
ENSP00000477968.1:p.Ala135Val
|
|
|
ENST00000644774.2:c.377C>T
|
ENSP00000493648.2:p.Ala126Val
|
|
|
ENST00000679410.1:n.528C>T
|
|
|
|
ENST00000679480.1:c.404C>T
|
ENSP00000506201.1:p.Ala135Val
|
|
|
ENST00000679535.1:n.705C>T
|
|
|
|
ENST00000679778.1:c.404C>T
|
ENSP00000505235.1:p.Ala135Val
|
|
|
ENST00000680227.1:c.404C>T
|
ENSP00000506253.1:p.Ala135Val
|
|
|
ENST00000680727.1:c.404C>T
|
ENSP00000505193.1:p.Ala135Val
|
|
|
ENST00000681052.1:c.404C>T
|
ENSP00000505060.1:p.Ala135Val
|
|
|
ENST00000681092.1:c.*208C>T
|
ENSP00000506720.1:n.*208C>T
|
|
|
ENST00000681842.1:c.404C>T
|
ENSP00000506126.1:p.Ala135Val
|
|
|
ENST00000331925.6:c.404C>T
|
ENSP00000331514.2:p.Ala135Val
|
|
|
ENST00000570382.1:c.340-8C>T
|
ENSP00000466346.1:n.340-8C>T
|
|
|
ENST00000571691.5:c.377C>T
|
ENSP00000461407.1:p.Ala126Val
|
|
|
ENST00000571721.5:c.404C>T
|
ENSP00000460660.1:p.Ala135Val
|
|
|
ENST00000572105.6:c.445C>T
|
ENSP00000462823.1:p.Pro149Ser
|
|
|
ENST00000573283.5:c.404C>T
|
ENSP00000458435.1:p.Ala135Val
|
|
|
ENST00000574671.5:n.263C>T
|
|
|
|
ENST00000575087.5:c.404C>T
|
ENSP00000459124.1:p.Ala135Val
|
|
|
ENST00000575659.5:c.404C>T
|
ENSP00000459119.1:p.Ala135Val
|
|
|
ENST00000575842.5:c.404C>T
|
ENSP00000458162.1:p.Ala135Val
|
|
|
ENST00000575994.5:c.404C>T
|
ENSP00000460464.1:p.Ala135Val
|
|
|
ENST00000576209.5:n.289C>T
|
|
|
|
ENST00000576214.2:n.602C>T
|
|
|
|
ENST00000576544.5:c.404C>T
|
ENSP00000461672.1:p.Ala135Val
|
|
|
ENST00000576917.5:n.457C>T
|
|
|
|
ENST00000615544.4:c.404C>T
|
ENSP00000477968.1:p.Ala135Val
|
|
|
NM_001199954.1:c.404C>T
|
NP_001186883.1:p.Ala135Val
|
|
|
NM_001614.3:c.404C>T
|
NP_001605.1:p.Ala135Val
|
|
|
NR_037688.1:n.543C>T
|
|
|
|
NM_001199954.2:c.404C>T
|
NP_001186883.1:p.Ala135Val
|
|
|
NM_001614.4:c.404C>T
|
NP_001605.1:p.Ala135Val
|
|
|
NR_037688.2:n.476C>T
|
|
|
|
NM_001614.5:c.404C>T
MANE Select
|
NP_001605.1:p.Ala135Val
|
|
|
NR_037688.3:n.476C>T
|
|
|
|
NM_001199954.3:c.404C>T
|
NP_001186883.1:p.Ala135Val
|
|
