ENST00000695651.1:n.2843G=
|
|
|
ENST00000695653.1:c.2404G=
|
ENSP00000512084.1:p.Asp802=
|
|
ENST00000695654.1:c.3520G=
|
ENSP00000512085.1:p.Asp1174=
|
|
ENST00000695689.1:c.466G=
|
ENSP00000512101.1:n.466G=
|
|
ENST00000695690.1:n.1560G=
|
|
|
ENST00000695691.1:n.1356G=
|
|
|
ENST00000245907.11:c.4495G=
MANE Select
|
ENSP00000245907.4:p.Asp1499=
|
|
ENST00000245907.10:c.4495G=
|
ENSP00000245907.4:p.Asp1499=
|
|
ENST00000599668.1:n.90G=
|
|
|
ENST00000599899.5:n.1454G=
|
|
|
ENST00000601008.1:c.242-1500G=
|
ENSP00000471384.1:n.242-1500G=
|
|
NM_000064.3:c.4495G=
|
NP_000055.2:p.Asp1499=
|
|
NM_000064.4:c.4495G=
MANE Select
|
NP_000055.2:p.Asp1499=
|
|