ENST00000695651.1:n.2902C>T
|
|
|
ENST00000695653.1:c.2463C>T
|
ENSP00000512084.1:p.Cys821=
|
|
ENST00000695654.1:c.3579C>T
|
ENSP00000512085.1:p.Cys1193=
|
|
ENST00000695689.1:c.525C>T
|
ENSP00000512101.1:n.525C>T
|
|
ENST00000695690.1:n.1619C>T
|
|
|
ENST00000695691.1:n.1415C>T
|
|
|
ENST00000245907.11:c.4554C>T
MANE Select
|
ENSP00000245907.4:p.Cys1518=
|
|
ENST00000245907.10:c.4554C>T
|
ENSP00000245907.4:p.Cys1518=
|
|
ENST00000599668.1:n.174C>T
|
|
|
ENST00000599899.5:n.1513C>T
|
|
|
ENST00000601008.1:c.242-1243C>T
|
ENSP00000471384.1:n.242-1243C>T
|
|
ENST00000602229.1:c.1C>T
|
|
|
NM_000064.3:c.4554C>T
|
NP_000055.2:p.Cys1518=
|
|
NM_000064.4:c.4554C>T
MANE Select
|
NP_000055.2:p.Cys1518=
|
|