ENST00000695651.1:n.1066C>G
|
|
|
ENST00000695652.1:c.2595C>G
|
ENSP00000512083.1:p.Gly865=
|
|
ENST00000695653.1:c.627C>G
|
ENSP00000512084.1:p.Gly209=
|
|
ENST00000695654.1:c.1842C>G
|
ENSP00000512085.1:p.Gly614=
|
|
ENST00000695655.1:c.1659C>G
|
ENSP00000512086.1:n.1659C>G
|
|
ENST00000695692.1:n.2082C>G
|
|
|
ENST00000245907.11:c.2718C>G
MANE Select
|
ENSP00000245907.4:p.Gly906=
|
|
ENST00000245907.10:c.2718C>G
|
ENSP00000245907.4:p.Gly906=
|
|
ENST00000594005.1:n.294C>G
|
|
|
NM_000064.3:c.2718C>G
|
NP_000055.2:p.Gly906=
|
|
NM_000064.4:c.2718C>G
MANE Select
|
NP_000055.2:p.Gly906=
|
|