ENST00000695651.1:n.2578C>G
|
|
|
ENST00000695653.1:c.2139C>G
|
ENSP00000512084.1:p.Gly713=
|
|
ENST00000695654.1:c.3255C>G
|
ENSP00000512085.1:p.Gly1085=
|
|
ENST00000695689.1:c.201C>G
|
ENSP00000512101.1:n.201C>G
|
|
ENST00000695690.1:n.421C>G
|
|
|
ENST00000695691.1:n.421C>G
|
|
|
ENST00000245907.11:c.4230C>G
MANE Select
|
ENSP00000245907.4:p.Gly1410=
|
|
ENST00000245907.10:c.4230C>G
|
ENSP00000245907.4:p.Gly1410=
|
|
ENST00000596548.1:c.351C>G
|
ENSP00000469744.1:p.Gly117=
|
|
ENST00000599899.5:n.1189C>G
|
|
|
ENST00000601008.1:c.242-4214C>G
|
ENSP00000471384.1:n.242-4214C>G
|
|
NM_000064.3:c.4230C>G
|
NP_000055.2:p.Gly1410=
|
|
NM_000064.4:c.4230C>G
MANE Select
|
NP_000055.2:p.Gly1410=
|
|