ENST00000608408.2:n.398+667G>A
(EAF1-AS1)
|
|
|
ENST00000626521.1:n.55+667G>A
(EAF1-AS1)
|
|
|
ENST00000629729.3:c.414+667G>A
|
ENSP00000518887.1:n.414+667G>A
|
|
ENST00000383788.10:c.*866G>A
(COLQ)
MANE Select
|
ENSP00000373298.3:n.*866G>A
|
|
ENST00000679838.1:c.*1996G>A
(COLQ)
|
ENSP00000505708.1:n.*1996G>A
|
|
ENST00000680545.1:n.2000G>A
(COLQ)
|
|
|
ENST00000680897.1:n.1699G>A
(COLQ)
|
|
|
ENST00000681097.1:c.*1248G>A
(COLQ)
|
ENSP00000505397.1:n.*1248G>A
|
|
ENST00000681222.1:n.5725G>A
(COLQ)
|
|
|
ENST00000383781.8:c.*866G>A
(COLQ)
|
ENSP00000373291.3:n.*866G>A
|
|
ENST00000383788.9:c.*866G>A
(COLQ)
|
ENSP00000373298.3:n.*866G>A
|
|
ENST00000603752.1:n.102G>A
(COLQ)
|
|
|
NM_005677.3:c.*866G>A
(COLQ)
|
NP_005668.2:n.*866G>A
|
|
NM_080538.2:c.*866G>A
(COLQ)
|
NP_536799.1:n.*866G>A
|
|
NM_080539.3:c.*866G>A
(COLQ)
|
NP_536800.2:n.*866G>A
|
|
NM_005677.4:c.*866G>A
(COLQ)
MANE Select
|
NP_005668.2:n.*866G>A
|
|
NM_080539.4:c.*866G>A
(COLQ)
|
NP_536800.2:n.*866G>A
|
|