ENST00000695652.1:c.1564-173C>T
|
ENSP00000512083.1:n.1564-173C>T
|
|
ENST00000695654.1:c.811-173C>T
|
ENSP00000512085.1:n.811-173C>T
|
|
ENST00000695655.1:c.592-137C>T
|
ENSP00000512086.1:n.592-137C>T
|
|
ENST00000695692.1:n.1051-173C>T
|
|
|
ENST00000245907.11:c.1687-173C>T
MANE Select
|
ENSP00000245907.4:n.1687-173C>T
|
|
ENST00000245907.10:c.1687-173C>T
|
ENSP00000245907.4:n.1687-173C>T
|
|
ENST00000600763.1:n.320-173C>T
|
|
|
NM_000064.3:c.1687-173C>T
|
NP_000055.2:n.1687-173C>T
|
|
NM_000064.4:c.1687-173C>T
MANE Select
|
NP_000055.2:n.1687-173C>T
|
|