ENST00000403665.7:c.1701G>T
(F11)
MANE Select
|
ENSP00000384957.2:p.Gly567=
|
|
ENST00000264691.4:c.301G>T
(F11)
|
|
|
ENST00000264692.8:c.1539G>T
(F11)
|
ENSP00000264692.5:p.Gly513=
|
|
ENST00000403665.6:c.1701G>T
(F11)
|
ENSP00000384957.2:p.Gly567=
|
|
ENST00000503841.1:n.220G>T
(F11)
|
|
|
NM_000128.3:c.1701G>T , LRG_583t1:c.1701G>T
(F11)
|
NP_000119.1:p.Gly567=
|
|
NR_033900.1:n.1066+620C>A
(F11-AS1)
|
|
|
XM_005262821.2:c.1704G>T
(F11)
|
XP_005262878.1:p.Gly568=
|
|
XM_005262822.2:c.1608G>T
(F11)
|
XP_005262879.1:p.Gly536=
|
|
XM_005262823.2:c.1434G>T
(F11)
|
XP_005262880.1:p.Gly478=
|
|
XM_006714137.1:c.1656G>T
(F11)
|
XP_006714200.1:p.Gly552=
|
|
XM_005262821.4:c.1704G>T
(F11)
|
XP_005262878.1:p.Gly568=
|
|
XM_005262822.4:c.1608G>T
(F11)
|
XP_005262879.1:p.Gly536=
|
|
XM_005262823.4:c.1434G>T
(F11)
|
XP_005262880.1:p.Gly478=
|
|
XM_006714137.3:c.1656G>T
(F11)
|
XP_006714200.1:p.Gly552=
|
|
NM_000128.4:c.1701G>T
(F11)
MANE Select
|
NP_000119.1:p.Gly567=
|
|