ENST00000695651.1:n.2937A>G
|
|
|
ENST00000695653.1:c.2498A>G
|
ENSP00000512084.1:p.Glu833Gly
|
|
ENST00000695654.1:c.3614A>G
|
ENSP00000512085.1:p.Glu1205Gly
|
|
ENST00000695689.1:c.560A>G
|
ENSP00000512101.1:n.560A>G
|
|
ENST00000695690.1:n.1654A>G
|
|
|
ENST00000695691.1:n.1450A>G
|
|
|
ENST00000245907.11:c.4589A>G
MANE Select
|
ENSP00000245907.4:p.Glu1530Gly
|
|
ENST00000245907.10:c.4589A>G
|
ENSP00000245907.4:p.Glu1530Gly
|
|
ENST00000599668.1:n.209A>G
|
|
|
ENST00000599899.5:n.1548A>G
|
|
|
ENST00000601008.1:c.242-1208A>G
|
ENSP00000471384.1:n.242-1208A>G
|
|
ENST00000602229.1:c.36A>G
|
|
|
NM_000064.3:c.4589A>G
|
NP_000055.2:p.Glu1530Gly
|
|
NM_000064.4:c.4589A>G
MANE Select
|
NP_000055.2:p.Glu1530Gly
|
|