ENST00000682565.1:c.10503A>T
|
ENSP00000507671.1:p.Arg3501=
|
|
ENST00000682801.1:c.10503A>T
|
ENSP00000507862.1:p.Arg3501=
|
|
ENST00000682859.1:c.10503A>T
|
ENSP00000508222.1:p.Arg3501=
|
|
ENST00000683791.1:c.3589A>T
|
|
|
ENST00000684460.1:c.7784A>T
|
|
|
ENST00000684548.1:c.10503A>T
|
ENSP00000507421.1:p.Arg3501=
|
|
ENST00000684590.1:c.4950A>T
|
ENSP00000507376.1:p.Arg1650=
|
|
ENST00000684656.1:c.7829A>T
|
|
|
ENST00000613296.6:c.10884A>T
MANE Select
|
ENSP00000482968.1:p.Arg3628=
|
|
ENST00000651057.1:c.1038A>T
|
ENSP00000498504.1:p.Arg346=
|
|
ENST00000651434.1:c.2240A>T
|
|
|
ENST00000651750.1:c.272A>T
|
|
|
ENST00000652487.1:c.1981A>T
|
|
|
ENST00000423048.5:c.4375A>T
|
ENSP00000399833.1:n.4375A>T
|
|
ENST00000484298.5:c.10758A>T
|
ENSP00000478155.1:p.Arg3586=
|
|
ENST00000613296.4:c.10884A>T
|
ENSP00000482968.1:p.Arg3628=
|
|
ENST00000614410.4:c.10884A>T
|
ENSP00000479094.1:p.Arg3628=
|
|
ENST00000620466.4:n.4687A>T
|
|
|
NM_015120.4:c.10887A>T , LRG_741t1:c.10887A>T
|
NP_055935.4:p.Arg3629=
|
|
NM_001378454.1:c.10884A>T
MANE Select
|
NP_001365383.1:p.Arg3628=
|
|