ENST00000695651.1:n.2945C>G
|
|
|
ENST00000695653.1:c.2506C>G
|
ENSP00000512084.1:p.Leu836Val
|
|
ENST00000695654.1:c.3622C>G
|
ENSP00000512085.1:p.Leu1208Val
|
|
ENST00000695689.1:c.568C>G
|
ENSP00000512101.1:n.568C>G
|
|
ENST00000695690.1:n.1662C>G
|
|
|
ENST00000695691.1:n.1458C>G
|
|
|
ENST00000245907.11:c.4597C>G
MANE Select
|
ENSP00000245907.4:p.Leu1533Val
|
|
ENST00000245907.10:c.4597C>G
|
ENSP00000245907.4:p.Leu1533Val
|
|
ENST00000599668.1:n.217C>G
|
|
|
ENST00000599899.5:n.1556C>G
|
|
|
ENST00000601008.1:c.242-1200C>G
|
ENSP00000471384.1:n.242-1200C>G
|
|
ENST00000602229.1:c.44C>G
|
|
|
NM_000064.3:c.4597C>G
|
NP_000055.2:p.Leu1533Val
|
|
NM_000064.4:c.4597C>G
MANE Select
|
NP_000055.2:p.Leu1533Val
|
|