ENST00000699749.1:c.736T>G
|
ENSP00000514559.1:p.Tyr246Asp
|
|
ENST00000699750.1:c.*664T>G
|
ENSP00000514560.1:n.*664T>G
|
|
ENST00000699751.1:n.1278+674T>G
|
|
|
ENST00000699779.1:c.*3673T>G
|
ENSP00000514585.1:n.*3673T>G
|
|
ENST00000699780.1:c.728+674T>G
|
ENSP00000514586.1:n.728+674T>G
|
|
ENST00000699781.1:c.*332+674T>G
|
ENSP00000514587.1:n.*332+674T>G
|
|
ENST00000699782.1:c.706T>G
|
ENSP00000514588.1:p.Tyr236Asp
|
|
ENST00000699783.1:c.775T>G
|
ENSP00000514589.1:p.Tyr259Asp
|
|
ENST00000699784.1:c.775T>G
|
ENSP00000514590.1:p.Tyr259Asp
|
|
ENST00000699785.1:c.*810T>G
|
ENSP00000514591.1:n.*810T>G
|
|
ENST00000373719.8:c.805T>G
MANE Select
|
ENSP00000362824.3:p.Tyr269Asp
|
|
ENST00000373701.7:c.775T>G
|
ENSP00000362805.3:p.Tyr259Asp
|
|
ENST00000373719.7:c.805T>G
|
ENSP00000362824.3:p.Tyr269Asp
|
|
ENST00000459760.1:n.182T>G
|
|
|
ENST00000488174.5:n.4165+674T>G
|
|
|
NM_181672.2:c.805T>G
|
NP_858058.1:p.Tyr269Asp
|
|
NM_181673.2:c.775T>G
|
NP_858059.1:p.Tyr259Asp
|
|
XM_005262308.1:c.-220+674T>G
|
XP_005262365.1:n.-220+674T>G
|
|
XM_017029908.1:c.-220+674T>G
|
XP_016885397.1:n.-220+674T>G
|
|
XM_024452467.1:c.-220+674T>G
|
XP_024308235.1:n.-220+674T>G
|
|
NM_181672.3:c.805T>G
MANE Select
|
NP_858058.1:p.Tyr269Asp
|
|
NM_181673.3:c.775T>G
|
NP_858059.1:p.Tyr259Asp
|
|