ENST00000695651.1:n.847G>A
|
|
|
ENST00000695652.1:c.2376G>A
|
ENSP00000512083.1:p.Leu792=
|
|
ENST00000695653.1:c.408G>A
|
ENSP00000512084.1:p.Leu136=
|
|
ENST00000695654.1:c.1623G>A
|
ENSP00000512085.1:p.Leu541=
|
|
ENST00000695655.1:c.1440G>A
|
ENSP00000512086.1:n.1440G>A
|
|
ENST00000695692.1:n.1863G>A
|
|
|
ENST00000245907.11:c.2499G>A
MANE Select
|
ENSP00000245907.4:p.Leu833=
|
|
ENST00000245907.10:c.2499G>A
|
ENSP00000245907.4:p.Leu833=
|
|
ENST00000602053.1:n.547G>A
|
|
|
NM_000064.3:c.2499G>A
|
NP_000055.2:p.Leu833=
|
|
NM_000064.4:c.2499G>A
MANE Select
|
NP_000055.2:p.Leu833=
|
|