ENST00000682565.1:c.7465C>A
|
ENSP00000507671.1:p.Arg2489=
|
|
ENST00000682801.1:c.7465C>A
|
ENSP00000507862.1:p.Arg2489=
|
|
ENST00000682859.1:c.7465C>A
|
ENSP00000508222.1:p.Arg2489=
|
|
ENST00000683791.1:c.857C>A
|
|
|
ENST00000684460.1:c.4917C>A
|
|
|
ENST00000684548.1:c.7465C>A
|
ENSP00000507421.1:p.Arg2489=
|
|
ENST00000684590.1:c.1912C>A
|
ENSP00000507376.1:p.Arg638=
|
|
ENST00000684656.1:c.4917C>A
|
|
|
ENST00000613296.6:c.7846C>A
MANE Select
|
ENSP00000482968.1:p.Arg2616=
|
|
ENST00000651434.1:c.896-29970C>A
|
|
|
ENST00000423048.5:c.2677C>A
|
ENSP00000399833.1:p.Arg893=
|
|
ENST00000484298.5:c.7720C>A
|
ENSP00000478155.1:p.Arg2574=
|
|
ENST00000613296.4:c.7846C>A
|
ENSP00000482968.1:p.Arg2616=
|
|
ENST00000614410.4:c.7846C>A
|
ENSP00000479094.1:p.Arg2616=
|
|
ENST00000620466.4:n.1649C>A
|
|
|
NM_015120.4:c.7849C>A , LRG_741t1:c.7849C>A
|
NP_055935.4:p.Arg2617=
|
|
NM_001378454.1:c.7846C>A
MANE Select
|
NP_001365383.1:p.Arg2616=
|
|