ENST00000695651.1:n.1999G=
|
|
|
ENST00000695652.1:c.3528G=
|
ENSP00000512083.1:p.Lys1176=
|
|
ENST00000695653.1:c.1560G=
|
ENSP00000512084.1:p.Lys520=
|
|
ENST00000695654.1:c.2676G=
|
ENSP00000512085.1:p.Lys892=
|
|
ENST00000695655.1:c.2592G=
|
ENSP00000512086.1:n.2592G=
|
|
ENST00000695692.1:n.3015G=
|
|
|
ENST00000245907.11:c.3651G=
MANE Select
|
ENSP00000245907.4:p.Lys1217=
|
|
ENST00000245907.10:c.3651G=
|
ENSP00000245907.4:p.Lys1217=
|
|
ENST00000596238.1:n.94G=
|
|
|
ENST00000601008.1:c.241+463G=
|
ENSP00000471384.1:n.241+463G=
|
|
NM_000064.3:c.3651G=
|
NP_000055.2:p.Lys1217=
|
|
NM_000064.4:c.3651G=
MANE Select
|
NP_000055.2:p.Lys1217=
|
|