ENST00000682565.1:c.7460G=
|
ENSP00000507671.1:p.Arg2487=
|
|
ENST00000682801.1:c.7460G=
|
ENSP00000507862.1:p.Arg2487=
|
|
ENST00000682859.1:c.7460G=
|
ENSP00000508222.1:p.Arg2487=
|
|
ENST00000683791.1:c.852G=
|
|
|
ENST00000684460.1:c.4912G=
|
|
|
ENST00000684548.1:c.7460G=
|
ENSP00000507421.1:p.Arg2487=
|
|
ENST00000684590.1:c.1907G=
|
ENSP00000507376.1:p.Arg636=
|
|
ENST00000684656.1:c.4912G=
|
|
|
ENST00000613296.6:c.7841G=
MANE Select
|
ENSP00000482968.1:p.Arg2614=
|
|
ENST00000651434.1:c.896-29975G=
|
|
|
ENST00000423048.5:c.2672G=
|
ENSP00000399833.1:p.Arg891=
|
|
ENST00000484298.5:c.7715G=
|
ENSP00000478155.1:p.Arg2572=
|
|
ENST00000613296.4:c.7841G=
|
ENSP00000482968.1:p.Arg2614=
|
|
ENST00000614410.4:c.7841G=
|
ENSP00000479094.1:p.Arg2614=
|
|
ENST00000620466.4:n.1644G=
|
|
|
NM_015120.4:c.7844G= , LRG_741t1:c.7844G=
|
NP_055935.4:p.Arg2615=
|
|
NM_001378454.1:c.7841G=
MANE Select
|
NP_001365383.1:p.Arg2614=
|
|