ENST00000403665.7:c.1594C>A
(F11)
MANE Select
|
ENSP00000384957.2:p.Leu532Ile
|
|
ENST00000264691.4:c.194C>A
(F11)
|
|
|
ENST00000264692.8:c.1432C>A
(F11)
|
ENSP00000264692.5:p.Leu478Ile
|
|
ENST00000403665.6:c.1594C>A
(F11)
|
ENSP00000384957.2:p.Leu532Ile
|
|
ENST00000503841.1:n.113C>A
(F11)
|
|
|
NM_000128.3:c.1594C>A , LRG_583t1:c.1594C>A
(F11)
|
NP_000119.1:p.Leu532Ile
|
|
NR_033900.1:n.1066+727G>T
(F11-AS1)
|
|
|
XM_005262821.2:c.1597C>A
(F11)
|
XP_005262878.1:p.Leu533Ile
|
|
XM_005262822.2:c.1501C>A
(F11)
|
XP_005262879.1:p.Leu501Ile
|
|
XM_005262823.2:c.1327C>A
(F11)
|
XP_005262880.1:p.Leu443Ile
|
|
XM_006714137.1:c.1549C>A
(F11)
|
XP_006714200.1:p.Leu517Ile
|
|
XR_938706.1:n.2002C>A
(F11)
|
|
|
XR_938707.1:n.1906C>A
(F11)
|
|
|
XM_005262821.4:c.1597C>A
(F11)
|
XP_005262878.1:p.Leu533Ile
|
|
XM_005262822.4:c.1501C>A
(F11)
|
XP_005262879.1:p.Leu501Ile
|
|
XM_005262823.4:c.1327C>A
(F11)
|
XP_005262880.1:p.Leu443Ile
|
|
XM_006714137.3:c.1549C>A
(F11)
|
XP_006714200.1:p.Leu517Ile
|
|
NM_000128.4:c.1594C>A
(F11)
MANE Select
|
NP_000119.1:p.Leu532Ile
|
|