ENST00000369538.4:c.819T>G
|
ENSP00000358551.4:p.Leu273=
|
|
ENST00000520113.7:c.831T>G
MANE Select
|
ENSP00000430075.3:p.Leu277=
|
|
ENST00000637080.1:c.614T>G
|
ENSP00000489753.1:n.614T>G
|
|
ENST00000639077.1:n.496T>G
|
|
|
ENST00000369538.3:c.918T>G
|
ENSP00000358551.3:p.Leu306=
|
|
ENST00000520113.6:c.930T>G
|
ENSP00000430075.2:p.Leu310=
|
|
NM_000036.2:c.930T>G
|
NP_000027.2:p.Leu310=
|
|
NM_001172626.1:c.918T>G
|
NP_001166097.1:p.Leu306=
|
|
NM_000036.3:c.831T>G
MANE Select
|
NP_000027.3:p.Leu277=
|
|
NM_001172626.2:c.819T>G
|
NP_001166097.2:p.Leu273=
|
|