ENST00000682565.1:c.7698A>G
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ENSP00000507671.1:p.Glu2566=
|
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ENST00000682801.1:c.7698A>G
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ENSP00000507862.1:p.Glu2566=
|
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ENST00000682859.1:c.7698A>G
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ENSP00000508222.1:p.Glu2566=
|
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ENST00000683791.1:c.1090A>G
|
|
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ENST00000684460.1:c.5150A>G
|
|
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ENST00000684548.1:c.7698A>G
|
ENSP00000507421.1:p.Glu2566=
|
|
ENST00000684590.1:c.2145A>G
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ENSP00000507376.1:p.Glu715=
|
|
ENST00000684656.1:c.5150A>G
|
|
|
ENST00000613296.6:c.8079A>G
MANE Select
|
ENSP00000482968.1:p.Glu2693=
|
|
ENST00000651434.1:c.896-29737A>G
|
|
|
ENST00000423048.5:c.2910A>G
|
ENSP00000399833.1:p.Glu970=
|
|
ENST00000484298.5:c.7953A>G
|
ENSP00000478155.1:p.Glu2651=
|
|
ENST00000613296.4:c.8079A>G
|
ENSP00000482968.1:p.Glu2693=
|
|
ENST00000614410.4:c.8079A>G
|
ENSP00000479094.1:p.Glu2693=
|
|
ENST00000620466.4:n.1882A>G
|
|
|
NM_015120.4:c.8082A>G , LRG_741t1:c.8082A>G
|
NP_055935.4:p.Glu2694=
|
|
NM_001378454.1:c.8079A>G
MANE Select
|
NP_001365383.1:p.Glu2693=
|
|