ENST00000695651.1:n.2071G>A
|
|
|
ENST00000695652.1:c.3600G>A
|
ENSP00000512083.1:p.Leu1200=
|
|
ENST00000695653.1:c.1632G>A
|
ENSP00000512084.1:p.Leu544=
|
|
ENST00000695654.1:c.2748G>A
|
ENSP00000512085.1:p.Leu916=
|
|
ENST00000695655.1:c.2664G>A
|
ENSP00000512086.1:n.2664G>A
|
|
ENST00000695692.1:n.3087G>A
|
|
|
ENST00000245907.11:c.3723G>A
MANE Select
|
ENSP00000245907.4:p.Leu1241=
|
|
ENST00000245907.10:c.3723G>A
|
ENSP00000245907.4:p.Leu1241=
|
|
ENST00000596238.1:n.166G>A
|
|
|
ENST00000601008.1:c.241+535G>A
|
ENSP00000471384.1:n.241+535G>A
|
|
NM_000064.3:c.3723G>A
|
NP_000055.2:p.Leu1241=
|
|
NM_000064.4:c.3723G>A
MANE Select
|
NP_000055.2:p.Leu1241=
|
|