ENST00000695651.1:n.788+626G>A
|
|
|
ENST00000695652.1:c.2317+626G>A
|
ENSP00000512083.1:n.2317+626G>A
|
|
ENST00000695653.1:c.349+626G>A
|
ENSP00000512084.1:n.349+626G>A
|
|
ENST00000695654.1:c.1564+626G>A
|
ENSP00000512085.1:n.1564+626G>A
|
|
ENST00000695655.1:c.1381+626G>A
|
ENSP00000512086.1:n.1381+626G>A
|
|
ENST00000695692.1:n.1804+626G>A
|
|
|
ENST00000245907.11:c.2440+626G>A
MANE Select
|
ENSP00000245907.4:n.2440+626G>A
|
|
ENST00000245907.10:c.2440+626G>A
|
ENSP00000245907.4:n.2440+626G>A
|
|
ENST00000602053.1:n.488+626G>A
|
|
|
NM_000064.3:c.2440+626G>A
|
NP_000055.2:n.2440+626G>A
|
|
NM_000064.4:c.2440+626G>A
MANE Select
|
NP_000055.2:n.2440+626G>A
|
|