ENST00000682028.1:c.477G=
|
ENSP00000507230.1:p.Gly159=
|
|
ENST00000682268.1:n.775G=
|
|
|
ENST00000682902.1:n.779G=
|
|
|
ENST00000683513.1:c.477G=
|
ENSP00000506809.1:p.Gly159=
|
|
ENST00000263431.4:c.477G=
MANE Select
|
ENSP00000263431.3:p.Gly159=
|
|
ENST00000263431.3:c.477G=
|
ENSP00000263431.3:p.Gly159=
|
|
ENST00000419486.1:c.93G=
|
ENSP00000387919.2:p.Gly31=
|
|
ENST00000474397.5:c.93G=
|
ENSP00000471271.1:p.Gly31=
|
|
NM_001316329.1:c.477G=
|
NP_001303258.1:p.Gly159=
|
|
NM_002739.3:c.477G= , LRG_669t1:c.477G=
|
NP_002730.1:p.Gly159=
|
|
NM_002739.4:c.477G=
|
NP_002730.1:p.Gly159=
|
|
NM_002739.5:c.477G=
MANE Select
|
NP_002730.1:p.Gly159=
|
|
NM_001316329.2:c.477G=
|
NP_001303258.1:p.Gly159=
|
|