ENST00000403665.7:c.1729G>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Gly577Arg
|
|
ENST00000264691.4:c.329G>C
(F11)
|
|
|
ENST00000264692.8:c.1567G>C
(F11)
|
ENSP00000264692.5:p.Gly523Arg
|
|
ENST00000403665.6:c.1729G>C
(F11)
|
ENSP00000384957.2:p.Gly577Arg
|
|
ENST00000503841.1:n.248G>C
(F11)
|
|
|
NM_000128.3:c.1729G>C , LRG_583t1:c.1729G>C
(F11)
|
NP_000119.1:p.Gly577Arg
|
|
NR_033900.1:n.1029C>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1732G>C
(F11)
|
XP_005262878.1:p.Gly578Arg
|
|
XM_005262822.2:c.1636G>C
(F11)
|
XP_005262879.1:p.Gly546Arg
|
|
XM_005262823.2:c.1462G>C
(F11)
|
XP_005262880.1:p.Gly488Arg
|
|
XM_006714137.1:c.1684G>C
(F11)
|
XP_006714200.1:p.Gly562Arg
|
|
XM_005262821.4:c.1732G>C
(F11)
|
XP_005262878.1:p.Gly578Arg
|
|
XM_005262822.4:c.1636G>C
(F11)
|
XP_005262879.1:p.Gly546Arg
|
|
XM_005262823.4:c.1462G>C
(F11)
|
XP_005262880.1:p.Gly488Arg
|
|
XM_006714137.3:c.1684G>C
(F11)
|
XP_006714200.1:p.Gly562Arg
|
|
NM_000128.4:c.1729G>C
(F11)
MANE Select
|
NP_000119.1:p.Gly577Arg
|
|