ENST00000403665.7:c.1809G>T
(F11)
MANE Select
|
ENSP00000384957.2:p.Glu603Asp
|
|
ENST00000264691.4:c.409G>T
(F11)
|
|
|
ENST00000264692.8:c.1647G>T
(F11)
|
ENSP00000264692.5:p.Glu549Asp
|
|
ENST00000403665.6:c.1809G>T
(F11)
|
ENSP00000384957.2:p.Glu603Asp
|
|
ENST00000503841.1:n.328G>T
(F11)
|
|
|
NM_000128.3:c.1809G>T , LRG_583t1:c.1809G>T
(F11)
|
NP_000119.1:p.Glu603Asp
|
|
NR_033900.1:n.949C>A
(F11-AS1)
|
|
|
XM_005262821.2:c.1812G>T
(F11)
|
XP_005262878.1:p.Glu604Asp
|
|
XM_005262822.2:c.1716G>T
(F11)
|
XP_005262879.1:p.Glu572Asp
|
|
XM_005262823.2:c.1542G>T
(F11)
|
XP_005262880.1:p.Glu514Asp
|
|
XM_006714137.1:c.1764G>T
(F11)
|
XP_006714200.1:p.Glu588Asp
|
|
XM_005262821.4:c.1812G>T
(F11)
|
XP_005262878.1:p.Glu604Asp
|
|
XM_005262822.4:c.1716G>T
(F11)
|
XP_005262879.1:p.Glu572Asp
|
|
XM_005262823.4:c.1542G>T
(F11)
|
XP_005262880.1:p.Glu514Asp
|
|
XM_006714137.3:c.1764G>T
(F11)
|
XP_006714200.1:p.Glu588Asp
|
|
NM_000128.4:c.1809G>T
(F11)
MANE Select
|
NP_000119.1:p.Glu603Asp
|
|