ENST00000378585.7:c.111G=
MANE Select
|
ENSP00000367848.4:p.Glu37=
|
|
ENST00000638411.1:c.111G=
|
ENSP00000491632.1:p.Glu37=
|
|
ENST00000638604.1:n.175G=
|
|
|
ENST00000638771.1:c.111G=
|
ENSP00000492435.1:p.Glu37=
|
|
ENST00000639045.1:c.*97G=
|
ENSP00000491997.1:n.*97G=
|
|
ENST00000639777.1:n.715G=
|
|
|
ENST00000639935.1:n.148G=
|
|
|
ENST00000640030.1:c.51G=
|
ENSP00000491411.1:p.Glu17=
|
|
ENST00000640067.1:c.111G=
|
ENSP00000491844.1:p.Glu37=
|
|
ENST00000640423.1:n.120G=
|
|
|
ENST00000640949.1:c.111G=
|
ENSP00000492500.1:p.Glu37=
|
|
ENST00000378585.5:c.111G=
|
ENSP00000367848.4:p.Glu37=
|
|
NM_000815.4:c.111G=
|
NP_000806.2:p.Glu37=
|
|
XM_011541194.1:c.150G=
|
XP_011539496.1:p.Glu50=
|
|
XM_011541194.3:c.150G=
|
XP_011539496.1:p.Glu50=
|
|
XM_017000936.1:c.816G=
|
XP_016856425.1:p.Glu272=
|
|
NM_000815.5:c.111G=
MANE Select
|
NP_000806.2:p.Glu37=
|
|