ENST00000307363.10:c.699G=
MANE Select
|
ENSP00000306920.4:p.Leu233=
|
|
ENST00000307363.9:c.699G=
|
ENSP00000306920.4:p.Leu233=
|
|
ENST00000307377.12:c.341-4574G=
|
ENSP00000305920.8:n.341-4574G=
|
|
ENST00000399402.7:c.609G=
|
ENSP00000382333.2:p.Leu203=
|
|
ENST00000415454.1:c.222G=
|
ENSP00000411813.1:p.Leu74=
|
|
ENST00000438227.1:c.*191G=
|
ENSP00000401250.1:n.*191G=
|
|
ENST00000440656.1:c.306G=
|
ENSP00000411769.1:p.Leu102=
|
|
ENST00000446732.5:c.*142G=
|
ENSP00000407365.1:n.*142G=
|
|
ENST00000482097.5:n.109-4574G=
|
|
|
ENST00000485698.5:n.137-4574G=
|
|
|
ENST00000498537.5:n.133-4574G=
|
|
|
NM_000404.2:c.699G=
|
NP_000395.2:p.Leu233=
|
|
NM_000404.3:c.699G=
|
NP_000395.2:p.Leu233=
|
|
NM_001079811.1:c.609G=
|
NP_001073279.1:p.Leu203=
|
|
NM_001079811.2:c.609G=
|
NP_001073279.1:p.Leu203=
|
|
NM_001135602.1:c.341-4574G=
|
NP_001129074.1:n.341-4574G=
|
|
NM_001135602.2:c.341-4574G=
|
NP_001129074.1:n.341-4574G=
|
|
NM_001317040.1:c.843G=
|
NP_001303969.1:p.Leu281=
|
|
NM_000404.4:c.699G=
MANE Select
|
NP_000395.3:p.Leu233=
|
|
NM_001079811.3:c.609G=
|
NP_001073279.2:p.Leu203=
|
|
NM_001135602.3:c.341-4574G=
|
NP_001129074.2:n.341-4574G=
|
|
NM_001317040.2:c.843G=
|
NP_001303969.2:p.Leu281=
|
|
NM_001393580.1:c.699G=
|
NP_001380509.1:p.Leu233=
|
|