ENST00000682565.1:c.10328A>G
|
ENSP00000507671.1:p.Tyr3443Cys
|
|
ENST00000682801.1:c.10328A>G
|
ENSP00000507862.1:p.Tyr3443Cys
|
|
ENST00000682859.1:c.10328A>G
|
ENSP00000508222.1:p.Tyr3443Cys
|
|
ENST00000683791.1:c.3414A>G
|
|
|
ENST00000684460.1:c.7609A>G
|
|
|
ENST00000684548.1:c.10328A>G
|
ENSP00000507421.1:p.Tyr3443Cys
|
|
ENST00000684590.1:c.4775A>G
|
ENSP00000507376.1:p.Tyr1592Cys
|
|
ENST00000684656.1:c.7654A>G
|
|
|
ENST00000613296.6:c.10709A>G
MANE Select
|
ENSP00000482968.1:p.Tyr3570Cys
|
|
ENST00000651057.1:c.863A>G
|
ENSP00000498504.1:p.Tyr288Cys
|
|
ENST00000651434.1:c.2065A>G
|
|
|
ENST00000651750.1:c.97A>G
|
|
|
ENST00000652487.1:c.1806A>G
|
|
|
ENST00000423048.5:c.4200A>G
|
ENSP00000399833.1:n.4200A>G
|
|
ENST00000484298.5:c.10583A>G
|
ENSP00000478155.1:p.Tyr3528Cys
|
|
ENST00000613296.4:c.10709A>G
|
ENSP00000482968.1:p.Tyr3570Cys
|
|
ENST00000614410.4:c.10709A>G
|
ENSP00000479094.1:p.Tyr3570Cys
|
|
ENST00000620466.4:n.4512A>G
|
|
|
NM_015120.4:c.10712A>G , LRG_741t1:c.10712A>G
|
NP_055935.4:p.Tyr3571Cys
|
|
NM_001378454.1:c.10709A>G
MANE Select
|
NP_001365383.1:p.Tyr3570Cys
|
|