ENST00000695651.1:n.2839G>A
|
|
|
ENST00000695653.1:c.2400G>A
|
ENSP00000512084.1:p.Lys800=
|
|
ENST00000695654.1:c.3516G>A
|
ENSP00000512085.1:p.Lys1172=
|
|
ENST00000695689.1:c.462G>A
|
ENSP00000512101.1:n.462G>A
|
|
ENST00000695690.1:n.1556G>A
|
|
|
ENST00000695691.1:n.1352G>A
|
|
|
ENST00000245907.11:c.4491G>A
MANE Select
|
ENSP00000245907.4:p.Lys1497=
|
|
ENST00000245907.10:c.4491G>A
|
ENSP00000245907.4:p.Lys1497=
|
|
ENST00000599668.1:n.86G>A
|
|
|
ENST00000599899.5:n.1450G>A
|
|
|
ENST00000601008.1:c.242-1504G>A
|
ENSP00000471384.1:n.242-1504G>A
|
|
NM_000064.3:c.4491G>A
|
NP_000055.2:p.Lys1497=
|
|
NM_000064.4:c.4491G>A
MANE Select
|
NP_000055.2:p.Lys1497=
|
|