ENST00000695651.1:n.2804+308T>G
|
|
|
ENST00000695653.1:c.2365+308T>G
|
ENSP00000512084.1:n.2365+308T>G
|
|
ENST00000695654.1:c.3481+308T>G
|
ENSP00000512085.1:n.3481+308T>G
|
|
ENST00000695689.1:c.427+308T>G
|
ENSP00000512101.1:n.427+308T>G
|
|
ENST00000695690.1:n.1521+308T>G
|
|
|
ENST00000695691.1:n.1317+308T>G
|
|
|
ENST00000245907.11:c.4456+308T>G
MANE Select
|
ENSP00000245907.4:n.4456+308T>G
|
|
ENST00000245907.10:c.4456+308T>G
|
ENSP00000245907.4:n.4456+308T>G
|
|
ENST00000599668.1:n.51+251T>G
|
|
|
ENST00000599899.5:n.1415+308T>G
|
|
|
ENST00000601008.1:c.242-1892T>G
|
ENSP00000471384.1:n.242-1892T>G
|
|
NM_000064.3:c.4456+308T>G
|
NP_000055.2:n.4456+308T>G
|
|
NM_000064.4:c.4456+308T>G
MANE Select
|
NP_000055.2:n.4456+308T>G
|
|