ENST00000246337.9:c.1005C>A
MANE Select
|
ENSP00000246337.4:p.Ala335=
|
|
ENST00000491773.6:c.762C>A
|
ENSP00000498551.1:p.Ala254=
|
|
ENST00000636293.1:c.867C>A
|
ENSP00000490710.1:p.Ala289=
|
|
ENST00000636836.1:c.*41C>A
|
ENSP00000490594.1:n.*41C>A
|
|
ENST00000651476.1:c.900C>A
|
ENSP00000498668.1:p.Ala300=
|
|
ENST00000652165.1:c.762C>A
|
ENSP00000498295.1:p.Ala254=
|
|
ENST00000652287.1:c.942C>A
|
ENSP00000498413.1:p.Ala314=
|
|
ENST00000652514.1:c.966C>A
|
ENSP00000498635.1:n.966C>A
|
|
ENST00000246337.8:c.1005C>A
|
ENSP00000246337.4:p.Ala335=
|
|
ENST00000465678.1:n.750C>A
|
|
|
ENST00000472254.1:n.758C>A
|
|
|
ENST00000494399.5:n.1672C>A
|
|
|
NM_000374.4:c.1005C>A
|
NP_000365.3:p.Ala335=
|
|
NR_036510.1:n.1188C>A
|
|
|
XM_005271169.1:c.789C>A
|
XP_005271226.1:p.Ala263=
|
|
XM_005271170.1:c.789C>A
|
XP_005271227.1:p.Ala263=
|
|
XM_011542080.1:c.942C>A
|
XP_011540382.1:p.Ala314=
|
|
XM_011542081.1:c.837C>A
|
XP_011540383.1:p.Ala279=
|
|
NM_000374.5:c.1005C>A
MANE Select
|
NP_000365.3:p.Ala335=
|
|
NR_158184.1:n.1086C>A
|
|
|
NR_158185.1:n.1036C>A
|
|
|
NR_036510.2:n.1067C>A
|
|
|