ENST00000699749.1:c.665T>G
|
ENSP00000514559.1:p.Val222Gly
|
|
ENST00000699750.1:c.*593T>G
|
ENSP00000514560.1:n.*593T>G
|
|
ENST00000699751.1:n.1278+603T>G
|
|
|
ENST00000699779.1:c.*3602T>G
|
ENSP00000514585.1:n.*3602T>G
|
|
ENST00000699780.1:c.728+603T>G
|
ENSP00000514586.1:n.728+603T>G
|
|
ENST00000699781.1:c.*332+603T>G
|
ENSP00000514587.1:n.*332+603T>G
|
|
ENST00000699782.1:c.635T>G
|
ENSP00000514588.1:p.Val212Gly
|
|
ENST00000699783.1:c.704T>G
|
ENSP00000514589.1:p.Val235Gly
|
|
ENST00000699784.1:c.704T>G
|
ENSP00000514590.1:p.Val235Gly
|
|
ENST00000699785.1:c.*739T>G
|
ENSP00000514591.1:n.*739T>G
|
|
ENST00000373719.8:c.734T>G
MANE Select
|
ENSP00000362824.3:p.Val245Gly
|
|
ENST00000373701.7:c.704T>G
|
ENSP00000362805.3:p.Val235Gly
|
|
ENST00000373719.7:c.734T>G
|
ENSP00000362824.3:p.Val245Gly
|
|
ENST00000455587.3:n.613T>G
|
|
|
ENST00000459760.1:n.111T>G
|
|
|
ENST00000488174.5:n.4165+603T>G
|
|
|
NM_181672.2:c.734T>G
|
NP_858058.1:p.Val245Gly
|
|
NM_181673.2:c.704T>G
|
NP_858059.1:p.Val235Gly
|
|
XM_005262308.1:c.-220+603T>G
|
XP_005262365.1:n.-220+603T>G
|
|
XM_017029908.1:c.-220+603T>G
|
XP_016885397.1:n.-220+603T>G
|
|
XM_024452467.1:c.-220+603T>G
|
XP_024308235.1:n.-220+603T>G
|
|
NM_181672.3:c.734T>G
MANE Select
|
NP_858058.1:p.Val245Gly
|
|
NM_181673.3:c.704T>G
|
NP_858059.1:p.Val235Gly
|
|