ENST00000293778.12:c.744G>C
MANE Select
|
ENSP00000293778.7:p.Val248=
|
|
ENST00000574412.6:c.744G>C
|
ENSP00000459592.2:p.Val248=
|
|
ENST00000293778.10:c.801G>C
|
ENSP00000293778.6:p.Val267=
|
|
ENST00000574412.5:c.801G>C
|
ENSP00000459592.1:p.Val267=
|
|
ENST00000575168.1:n.575G>C
|
|
|
ENST00000576153.5:n.535G>C
|
|
|
NM_001100812.1:c.801G>C
|
NP_001094282.1:p.Val267=
|
|
NM_022059.3:c.801G>C
|
NP_071342.2:p.Val267=
|
|
NM_022059.4:c.801G>C
|
NP_071342.2:p.Val267=
|
|
NM_001100812.2:c.744G>C
|
NP_001094282.2:p.Val248=
|
|
NM_001386809.1:c.744G>C
MANE Select
|
NP_001373738.1:p.Val248=
|
|