ENST00000682565.1:c.10436G=
|
ENSP00000507671.1:p.Arg3479=
|
|
ENST00000682801.1:c.10436G=
|
ENSP00000507862.1:p.Arg3479=
|
|
ENST00000682859.1:c.10436G=
|
ENSP00000508222.1:p.Arg3479=
|
|
ENST00000683791.1:c.3522G=
|
|
|
ENST00000684460.1:c.7717G=
|
|
|
ENST00000684548.1:c.10436G=
|
ENSP00000507421.1:p.Arg3479=
|
|
ENST00000684590.1:c.4883G=
|
ENSP00000507376.1:p.Arg1628=
|
|
ENST00000684656.1:c.7762G=
|
|
|
ENST00000613296.6:c.10817G=
MANE Select
|
ENSP00000482968.1:p.Arg3606=
|
|
ENST00000651057.1:c.971G=
|
ENSP00000498504.1:p.Arg324=
|
|
ENST00000651434.1:c.2173G=
|
|
|
ENST00000651750.1:c.205G=
|
|
|
ENST00000652487.1:c.1914G=
|
|
|
ENST00000423048.5:c.4308G=
|
ENSP00000399833.1:n.4308G=
|
|
ENST00000484298.5:c.10691G=
|
ENSP00000478155.1:p.Arg3564=
|
|
ENST00000613296.4:c.10817G=
|
ENSP00000482968.1:p.Arg3606=
|
|
ENST00000614410.4:c.10817G=
|
ENSP00000479094.1:p.Arg3606=
|
|
ENST00000620466.4:n.4620G=
|
|
|
NM_015120.4:c.10820G= , LRG_741t1:c.10820G=
|
NP_055935.4:p.Arg3607=
|
|
NM_001378454.1:c.10817G=
MANE Select
|
NP_001365383.1:p.Arg3606=
|
|