ENST00000682565.1:c.11602A>T
|
ENSP00000507671.1:p.Arg3868Ter
|
|
ENST00000682801.1:c.11167-880A>T
|
ENSP00000507862.1:n.11167-880A>T
|
|
ENST00000682859.1:c.11602A>T
|
ENSP00000508222.1:p.Arg3868Ter
|
|
ENST00000683791.1:c.4688A>T
|
|
|
ENST00000684460.1:c.8883A>T
|
|
|
ENST00000684548.1:c.11602A>T
|
ENSP00000507421.1:p.Arg3868Ter
|
|
ENST00000684590.1:c.6049A>T
|
ENSP00000507376.1:p.Arg2017Ter
|
|
ENST00000684656.1:c.9067A>T
|
|
|
ENST00000613296.6:c.11983A>T
MANE Select
|
ENSP00000482968.1:p.Arg3995Ter
|
|
ENST00000651057.1:c.2137A>T
|
ENSP00000498504.1:p.Arg713Ter
|
|
ENST00000651434.1:c.3339A>T
|
|
|
ENST00000651750.1:c.1260+424A>T
|
|
|
ENST00000652487.1:c.3154A>T
|
|
|
ENST00000464408.3:n.158A>T
|
|
|
ENST00000484298.5:c.11857A>T
|
ENSP00000478155.1:p.Arg3953Ter
|
|
ENST00000613296.4:c.11983A>T
|
ENSP00000482968.1:p.Arg3995Ter
|
|
ENST00000620466.4:n.5786A>T
|
|
|
NM_015120.4:c.11986A>T , LRG_741t1:c.11986A>T
|
NP_055935.4:p.Arg3996Ter
|
|
NM_001378454.1:c.11983A>T
MANE Select
|
NP_001365383.1:p.Arg3995Ter
|
|