ENST00000695651.1:n.2917G>T
|
|
|
ENST00000695653.1:c.2478G>T
|
ENSP00000512084.1:p.Ser826=
|
|
ENST00000695654.1:c.3594G>T
|
ENSP00000512085.1:p.Ser1198=
|
|
ENST00000695689.1:c.540G>T
|
ENSP00000512101.1:n.540G>T
|
|
ENST00000695690.1:n.1634G>T
|
|
|
ENST00000695691.1:n.1430G>T
|
|
|
ENST00000245907.11:c.4569G>T
MANE Select
|
ENSP00000245907.4:p.Ser1523=
|
|
ENST00000245907.10:c.4569G>T
|
ENSP00000245907.4:p.Ser1523=
|
|
ENST00000599668.1:n.189G>T
|
|
|
ENST00000599899.5:n.1528G>T
|
|
|
ENST00000601008.1:c.242-1228G>T
|
ENSP00000471384.1:n.242-1228G>T
|
|
ENST00000602229.1:c.16G>T
|
|
|
NM_000064.3:c.4569G>T
|
NP_000055.2:p.Ser1523=
|
|
NM_000064.4:c.4569G>T
MANE Select
|
NP_000055.2:p.Ser1523=
|
|