ENST00000691183.1:c.*460A>T
|
ENSP00000509954.1:n.*460A>T
|
|
ENST00000378842.8:c.872A>T
MANE Select
|
ENSP00000368119.4:p.Glu291Val
|
|
ENST00000378842.7:c.872A>T
|
ENSP00000368119.3:p.Glu291Val
|
|
ENST00000450095.6:c.545A>T
|
ENSP00000401956.2:p.Glu182Val
|
|
ENST00000488412.2:n.128A>T
|
|
|
ENST00000489643.6:n.952A>T
|
|
|
ENST00000554550.5:c.*492A>T
|
ENSP00000451435.1:n.*492A>T
|
|
ENST00000554638.5:n.1344A>T
|
|
|
ENST00000555020.5:n.1333A>T
|
|
|
ENST00000555086.5:n.979A>T
|
|
|
ENST00000555754.1:n.320A>T
|
|
|
ENST00000556278.1:c.432+593A>T
|
ENSP00000451792.1:n.432+593A>T
|
|
ENST00000557706.5:n.1447A>T
|
|
|
NM_000155.3:c.872A>T
|
NP_000146.2:p.Glu291Val
|
|
NM_001258332.1:c.545A>T
|
NP_001245261.1:p.Glu182Val
|
|
NM_000155.4:c.872A>T
MANE Select
|
NP_000146.2:p.Glu291Val
|
|
NM_001258332.2:c.545A>T
|
NP_001245261.1:p.Glu182Val
|
|