ENST00000682565.1:c.11602A>G
|
ENSP00000507671.1:p.Arg3868Gly
|
|
ENST00000682801.1:c.11167-880A>G
|
ENSP00000507862.1:n.11167-880A>G
|
|
ENST00000682859.1:c.11602A>G
|
ENSP00000508222.1:p.Arg3868Gly
|
|
ENST00000683791.1:c.4688A>G
|
|
|
ENST00000684460.1:c.8883A>G
|
|
|
ENST00000684548.1:c.11602A>G
|
ENSP00000507421.1:p.Arg3868Gly
|
|
ENST00000684590.1:c.6049A>G
|
ENSP00000507376.1:p.Arg2017Gly
|
|
ENST00000684656.1:c.9067A>G
|
|
|
ENST00000613296.6:c.11983A>G
MANE Select
|
ENSP00000482968.1:p.Arg3995Gly
|
|
ENST00000651057.1:c.2137A>G
|
ENSP00000498504.1:p.Arg713Gly
|
|
ENST00000651434.1:c.3339A>G
|
|
|
ENST00000651750.1:c.1260+424A>G
|
|
|
ENST00000652487.1:c.3154A>G
|
|
|
ENST00000464408.3:n.158A>G
|
|
|
ENST00000484298.5:c.11857A>G
|
ENSP00000478155.1:p.Arg3953Gly
|
|
ENST00000613296.4:c.11983A>G
|
ENSP00000482968.1:p.Arg3995Gly
|
|
ENST00000620466.4:n.5786A>G
|
|
|
NM_015120.4:c.11986A>G , LRG_741t1:c.11986A>G
|
NP_055935.4:p.Arg3996Gly
|
|
NM_001378454.1:c.11983A>G
MANE Select
|
NP_001365383.1:p.Arg3995Gly
|
|