ENST00000682565.1:c.10447A>C
|
ENSP00000507671.1:p.Arg3483=
|
|
ENST00000682801.1:c.10447A>C
|
ENSP00000507862.1:p.Arg3483=
|
|
ENST00000682859.1:c.10447A>C
|
ENSP00000508222.1:p.Arg3483=
|
|
ENST00000683791.1:c.3533A>C
|
|
|
ENST00000684460.1:c.7728A>C
|
|
|
ENST00000684548.1:c.10447A>C
|
ENSP00000507421.1:p.Arg3483=
|
|
ENST00000684590.1:c.4894A>C
|
ENSP00000507376.1:p.Arg1632=
|
|
ENST00000684656.1:c.7773A>C
|
|
|
ENST00000613296.6:c.10828A>C
MANE Select
|
ENSP00000482968.1:p.Arg3610=
|
|
ENST00000651057.1:c.982A>C
|
ENSP00000498504.1:p.Arg328=
|
|
ENST00000651434.1:c.2184A>C
|
|
|
ENST00000651750.1:c.216A>C
|
|
|
ENST00000652487.1:c.1925A>C
|
|
|
ENST00000423048.5:c.4319A>C
|
ENSP00000399833.1:n.4319A>C
|
|
ENST00000484298.5:c.10702A>C
|
ENSP00000478155.1:p.Arg3568=
|
|
ENST00000613296.4:c.10828A>C
|
ENSP00000482968.1:p.Arg3610=
|
|
ENST00000614410.4:c.10828A>C
|
ENSP00000479094.1:p.Arg3610=
|
|
ENST00000620466.4:n.4631A>C
|
|
|
NM_015120.4:c.10831A>C , LRG_741t1:c.10831A>C
|
NP_055935.4:p.Arg3611=
|
|
NM_001378454.1:c.10828A>C
MANE Select
|
NP_001365383.1:p.Arg3610=
|
|