ENST00000682565.1:c.10380C>T
|
ENSP00000507671.1:p.Thr3460=
|
|
ENST00000682801.1:c.10380C>T
|
ENSP00000507862.1:p.Thr3460=
|
|
ENST00000682859.1:c.10380C>T
|
ENSP00000508222.1:p.Thr3460=
|
|
ENST00000683791.1:c.3466C>T
|
|
|
ENST00000684460.1:c.7661C>T
|
|
|
ENST00000684548.1:c.10380C>T
|
ENSP00000507421.1:p.Thr3460=
|
|
ENST00000684590.1:c.4827C>T
|
ENSP00000507376.1:p.Thr1609=
|
|
ENST00000684656.1:c.7706C>T
|
|
|
ENST00000613296.6:c.10761C>T
MANE Select
|
ENSP00000482968.1:p.Thr3587=
|
|
ENST00000651057.1:c.915C>T
|
ENSP00000498504.1:p.Thr305=
|
|
ENST00000651434.1:c.2117C>T
|
|
|
ENST00000651750.1:c.149C>T
|
|
|
ENST00000652487.1:c.1858C>T
|
|
|
ENST00000423048.5:c.4252C>T
|
ENSP00000399833.1:n.4252C>T
|
|
ENST00000484298.5:c.10635C>T
|
ENSP00000478155.1:p.Thr3545=
|
|
ENST00000613296.4:c.10761C>T
|
ENSP00000482968.1:p.Thr3587=
|
|
ENST00000614410.4:c.10761C>T
|
ENSP00000479094.1:p.Thr3587=
|
|
ENST00000620466.4:n.4564C>T
|
|
|
NM_015120.4:c.10764C>T , LRG_741t1:c.10764C>T
|
NP_055935.4:p.Thr3588=
|
|
NM_001378454.1:c.10761C>T
MANE Select
|
NP_001365383.1:p.Thr3587=
|
|