ENST00000699749.1:c.743A>T
|
ENSP00000514559.1:p.Glu248Val
|
|
ENST00000699750.1:c.*671A>T
|
ENSP00000514560.1:n.*671A>T
|
|
ENST00000699751.1:n.1278+681A>T
|
|
|
ENST00000699779.1:c.*3680A>T
|
ENSP00000514585.1:n.*3680A>T
|
|
ENST00000699780.1:c.729-681A>T
|
ENSP00000514586.1:n.729-681A>T
|
|
ENST00000699781.1:c.*333-681A>T
|
ENSP00000514587.1:n.*333-681A>T
|
|
ENST00000699782.1:c.713A>T
|
ENSP00000514588.1:p.Glu238Val
|
|
ENST00000699783.1:c.782A>T
|
ENSP00000514589.1:p.Glu261Val
|
|
ENST00000699784.1:c.782A>T
|
ENSP00000514590.1:p.Glu261Val
|
|
ENST00000699785.1:c.*817A>T
|
ENSP00000514591.1:n.*817A>T
|
|
ENST00000373719.8:c.812A>T
MANE Select
|
ENSP00000362824.3:p.Glu271Val
|
|
ENST00000373701.7:c.782A>T
|
ENSP00000362805.3:p.Glu261Val
|
|
ENST00000373719.7:c.812A>T
|
ENSP00000362824.3:p.Glu271Val
|
|
ENST00000459760.1:n.189A>T
|
|
|
ENST00000488174.5:n.4166-681A>T
|
|
|
NM_181672.2:c.812A>T
|
NP_858058.1:p.Glu271Val
|
|
NM_181673.2:c.782A>T
|
NP_858059.1:p.Glu261Val
|
|
XM_005262308.1:c.-219-681A>T
|
XP_005262365.1:n.-219-681A>T
|
|
XM_017029908.1:c.-219-681A>T
|
XP_016885397.1:n.-219-681A>T
|
|
XM_024452467.1:c.-219-681A>T
|
XP_024308235.1:n.-219-681A>T
|
|
NM_181672.3:c.812A>T
MANE Select
|
NP_858058.1:p.Glu271Val
|
|
NM_181673.3:c.782A>T
|
NP_858059.1:p.Glu261Val
|
|