ENST00000682028.1:c.111G=
|
ENSP00000507230.1:p.Lys37=
|
|
ENST00000682268.1:n.409G=
|
|
|
ENST00000682902.1:n.413G=
|
|
|
ENST00000683513.1:c.111G=
|
ENSP00000506809.1:p.Lys37=
|
|
ENST00000263431.4:c.111G=
MANE Select
|
ENSP00000263431.3:p.Lys37=
|
|
ENST00000263431.3:c.111G=
|
ENSP00000263431.3:p.Lys37=
|
|
ENST00000419486.1:c.-274G=
|
ENSP00000387919.2:n.-274G=
|
|
ENST00000474397.5:c.-274G=
|
ENSP00000471271.1:n.-274G=
|
|
ENST00000479081.5:c.-274G=
|
ENSP00000471544.1:n.-274G=
|
|
NM_001316329.1:c.111G=
|
NP_001303258.1:p.Lys37=
|
|
NM_002739.3:c.111G= , LRG_669t1:c.111G=
|
NP_002730.1:p.Lys37=
|
|
NM_002739.4:c.111G=
|
NP_002730.1:p.Lys37=
|
|
NM_002739.5:c.111G=
MANE Select
|
NP_002730.1:p.Lys37=
|
|
NM_001316329.2:c.111G=
|
NP_001303258.1:p.Lys37=
|
|