ENST00000699749.1:c.675T>G
|
ENSP00000514559.1:p.Tyr225Ter
|
|
ENST00000699750.1:c.*603T>G
|
ENSP00000514560.1:n.*603T>G
|
|
ENST00000699751.1:n.1278+613T>G
|
|
|
ENST00000699779.1:c.*3612T>G
|
ENSP00000514585.1:n.*3612T>G
|
|
ENST00000699780.1:c.728+613T>G
|
ENSP00000514586.1:n.728+613T>G
|
|
ENST00000699781.1:c.*332+613T>G
|
ENSP00000514587.1:n.*332+613T>G
|
|
ENST00000699782.1:c.645T>G
|
ENSP00000514588.1:p.Tyr215Ter
|
|
ENST00000699783.1:c.714T>G
|
ENSP00000514589.1:p.Tyr238Ter
|
|
ENST00000699784.1:c.714T>G
|
ENSP00000514590.1:p.Tyr238Ter
|
|
ENST00000699785.1:c.*749T>G
|
ENSP00000514591.1:n.*749T>G
|
|
ENST00000373719.8:c.744T>G
MANE Select
|
ENSP00000362824.3:p.Tyr248Ter
|
|
ENST00000373701.7:c.714T>G
|
ENSP00000362805.3:p.Tyr238Ter
|
|
ENST00000373719.7:c.744T>G
|
ENSP00000362824.3:p.Tyr248Ter
|
|
ENST00000455587.3:n.623T>G
|
|
|
ENST00000459760.1:n.121T>G
|
|
|
ENST00000488174.5:n.4165+613T>G
|
|
|
NM_181672.2:c.744T>G
|
NP_858058.1:p.Tyr248Ter
|
|
NM_181673.2:c.714T>G
|
NP_858059.1:p.Tyr238Ter
|
|
XM_005262308.1:c.-220+613T>G
|
XP_005262365.1:n.-220+613T>G
|
|
XM_017029908.1:c.-220+613T>G
|
XP_016885397.1:n.-220+613T>G
|
|
XM_024452467.1:c.-220+613T>G
|
XP_024308235.1:n.-220+613T>G
|
|
NM_181672.3:c.744T>G
MANE Select
|
NP_858058.1:p.Tyr248Ter
|
|
NM_181673.3:c.714T>G
|
NP_858059.1:p.Tyr238Ter
|
|