ENST00000570382.2:c.665A>T
|
ENSP00000466346.2:p.Asp222Val
|
|
ENST00000571691.6:c.593A>T
|
ENSP00000461407.2:p.Asp198Val
|
|
ENST00000571721.6:c.665A>T
|
ENSP00000460660.2:p.Asp222Val
|
|
ENST00000572105.7:c.*109A>T
|
ENSP00000462823.1:n.*109A>T
|
|
ENST00000573283.7:c.665A>T
MANE Select
|
ENSP00000458435.1:p.Asp222Val
|
|
ENST00000574671.6:n.1065A>T
|
|
|
ENST00000575659.6:c.665A>T
|
ENSP00000459119.2:p.Asp222Val
|
|
ENST00000575994.6:c.665A>T
|
ENSP00000460464.2:p.Asp222Val
|
|
ENST00000576214.3:n.966A>T
|
|
|
ENST00000576544.6:c.665A>T
|
ENSP00000461672.1:p.Asp222Val
|
|
ENST00000615544.5:c.665A>T
|
ENSP00000477968.1:p.Asp222Val
|
|
ENST00000644774.2:c.638A>T
|
ENSP00000493648.2:p.Asp213Val
|
|
ENST00000679410.1:n.789A>T
|
|
|
ENST00000679480.1:c.665A>T
|
ENSP00000506201.1:p.Asp222Val
|
|
ENST00000679535.1:n.966A>T
|
|
|
ENST00000679778.1:c.665A>T
|
ENSP00000505235.1:p.Asp222Val
|
|
ENST00000680227.1:c.665A>T
|
ENSP00000506253.1:p.Asp222Val
|
|
ENST00000680727.1:c.665A>T
|
ENSP00000505193.1:p.Asp222Val
|
|
ENST00000681052.1:c.665A>T
|
ENSP00000505060.1:p.Asp222Val
|
|
ENST00000681092.1:c.*469A>T
|
ENSP00000506720.1:n.*469A>T
|
|
ENST00000681842.1:c.665A>T
|
ENSP00000506126.1:p.Asp222Val
|
|
ENST00000331925.6:c.665A>T
|
ENSP00000331514.2:p.Asp222Val
|
|
ENST00000571691.5:c.638A>T
|
ENSP00000461407.1:p.Asp213Val
|
|
ENST00000572105.6:c.*109A>T
|
ENSP00000462823.1:n.*109A>T
|
|
ENST00000573283.5:c.665A>T
|
ENSP00000458435.1:p.Asp222Val
|
|
ENST00000574671.5:n.524A>T
|
|
|
ENST00000575087.5:c.665A>T
|
ENSP00000459124.1:p.Asp222Val
|
|
ENST00000575842.5:c.665A>T
|
ENSP00000458162.1:p.Asp222Val
|
|
ENST00000576209.5:n.550A>T
|
|
|
ENST00000576214.2:n.863A>T
|
|
|
ENST00000576544.5:c.665A>T
|
ENSP00000461672.1:p.Asp222Val
|
|
ENST00000576917.5:n.718A>T
|
|
|
ENST00000615544.4:c.665A>T
|
ENSP00000477968.1:p.Asp222Val
|
|
NM_001199954.1:c.665A>T
|
NP_001186883.1:p.Asp222Val
|
|
NM_001614.3:c.665A>T
|
NP_001605.1:p.Asp222Val
|
|
NR_037688.1:n.804A>T
|
|
|
NM_001199954.2:c.665A>T
|
NP_001186883.1:p.Asp222Val
|
|
NM_001614.4:c.665A>T
|
NP_001605.1:p.Asp222Val
|
|
NR_037688.2:n.737A>T
|
|
|
NM_001614.5:c.665A>T
MANE Select
|
NP_001605.1:p.Asp222Val
|
|
NR_037688.3:n.737A>T
|
|
|
NM_001199954.3:c.665A>T
|
NP_001186883.1:p.Asp222Val
|
|