ENST00000403665.7:c.1803A>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Gln601His
|
|
ENST00000264691.4:c.403A>C
(F11)
|
|
|
ENST00000264692.8:c.1641A>C
(F11)
|
ENSP00000264692.5:p.Gln547His
|
|
ENST00000403665.6:c.1803A>C
(F11)
|
ENSP00000384957.2:p.Gln601His
|
|
ENST00000503841.1:n.322A>C
(F11)
|
|
|
NM_000128.3:c.1803A>C , LRG_583t1:c.1803A>C
(F11)
|
NP_000119.1:p.Gln601His
|
|
NR_033900.1:n.955T>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1806A>C
(F11)
|
XP_005262878.1:p.Gln602His
|
|
XM_005262822.2:c.1710A>C
(F11)
|
XP_005262879.1:p.Gln570His
|
|
XM_005262823.2:c.1536A>C
(F11)
|
XP_005262880.1:p.Gln512His
|
|
XM_006714137.1:c.1758A>C
(F11)
|
XP_006714200.1:p.Gln586His
|
|
XM_005262821.4:c.1806A>C
(F11)
|
XP_005262878.1:p.Gln602His
|
|
XM_005262822.4:c.1710A>C
(F11)
|
XP_005262879.1:p.Gln570His
|
|
XM_005262823.4:c.1536A>C
(F11)
|
XP_005262880.1:p.Gln512His
|
|
XM_006714137.3:c.1758A>C
(F11)
|
XP_006714200.1:p.Gln586His
|
|
NM_000128.4:c.1803A>C
(F11)
MANE Select
|
NP_000119.1:p.Gln601His
|
|