ENST00000682565.1:c.10627A>T
|
ENSP00000507671.1:p.Arg3543Ter
|
|
ENST00000682801.1:c.10627A>T
|
ENSP00000507862.1:p.Arg3543Ter
|
|
ENST00000682859.1:c.10627A>T
|
ENSP00000508222.1:p.Arg3543Ter
|
|
ENST00000683791.1:c.3713A>T
|
|
|
ENST00000684460.1:c.7908A>T
|
|
|
ENST00000684548.1:c.10627A>T
|
ENSP00000507421.1:p.Arg3543Ter
|
|
ENST00000684590.1:c.5074A>T
|
ENSP00000507376.1:p.Arg1692Ter
|
|
ENST00000684656.1:c.7953A>T
|
|
|
ENST00000613296.6:c.11008A>T
MANE Select
|
ENSP00000482968.1:p.Arg3670Ter
|
|
ENST00000651057.1:c.1162A>T
|
ENSP00000498504.1:p.Arg388Ter
|
|
ENST00000651434.1:c.2364A>T
|
|
|
ENST00000651750.1:c.396A>T
|
|
|
ENST00000652487.1:c.2105A>T
|
|
|
ENST00000423048.5:c.4499A>T
|
ENSP00000399833.1:n.4499A>T
|
|
ENST00000484298.5:c.10882A>T
|
ENSP00000478155.1:p.Arg3628Ter
|
|
ENST00000613296.4:c.11008A>T
|
ENSP00000482968.1:p.Arg3670Ter
|
|
ENST00000614410.4:c.11008A>T
|
ENSP00000479094.1:p.Arg3670Ter
|
|
ENST00000620466.4:n.4811A>T
|
|
|
NM_015120.4:c.11011A>T , LRG_741t1:c.11011A>T
|
NP_055935.4:p.Arg3671Ter
|
|
NM_001378454.1:c.11008A>T
MANE Select
|
NP_001365383.1:p.Arg3670Ter
|
|