ENST00000695651.1:n.2866C>T
|
|
|
ENST00000695653.1:c.2427C>T
|
ENSP00000512084.1:p.Cys809=
|
|
ENST00000695654.1:c.3543C>T
|
ENSP00000512085.1:p.Cys1181=
|
|
ENST00000695689.1:c.489C>T
|
ENSP00000512101.1:n.489C>T
|
|
ENST00000695690.1:n.1583C>T
|
|
|
ENST00000695691.1:n.1379C>T
|
|
|
ENST00000245907.11:c.4518C>T
MANE Select
|
ENSP00000245907.4:p.Cys1506=
|
|
ENST00000245907.10:c.4518C>T
|
ENSP00000245907.4:p.Cys1506=
|
|
ENST00000599668.1:n.113C>T
|
|
|
ENST00000599899.5:n.1477C>T
|
|
|
ENST00000601008.1:c.242-1477C>T
|
ENSP00000471384.1:n.242-1477C>T
|
|
NM_000064.3:c.4518C>T
|
NP_000055.2:p.Cys1506=
|
|
NM_000064.4:c.4518C>T
MANE Select
|
NP_000055.2:p.Cys1506=
|
|