ENST00000403665.7:c.1869A>T
(F11)
MANE Select
|
ENSP00000384957.2:p.Gln623His
|
|
ENST00000264691.4:c.469A>T
(F11)
|
|
|
ENST00000264692.8:c.1707A>T
(F11)
|
ENSP00000264692.5:p.Gln569His
|
|
ENST00000403665.6:c.1869A>T
(F11)
|
ENSP00000384957.2:p.Gln623His
|
|
ENST00000503841.1:n.388A>T
(F11)
|
|
|
NM_000128.3:c.1869A>T , LRG_583t1:c.1869A>T
(F11)
|
NP_000119.1:p.Gln623His
|
|
NR_033900.1:n.889T>A
(F11-AS1)
|
|
|
XM_005262821.2:c.1872A>T
(F11)
|
XP_005262878.1:p.Gln624His
|
|
XM_005262822.2:c.1776A>T
(F11)
|
XP_005262879.1:p.Gln592His
|
|
XM_005262823.2:c.1602A>T
(F11)
|
XP_005262880.1:p.Gln534His
|
|
XM_006714137.1:c.1824A>T
(F11)
|
XP_006714200.1:p.Gln608His
|
|
XM_005262821.4:c.1872A>T
(F11)
|
XP_005262878.1:p.Gln624His
|
|
XM_005262822.4:c.1776A>T
(F11)
|
XP_005262879.1:p.Gln592His
|
|
XM_005262823.4:c.1602A>T
(F11)
|
XP_005262880.1:p.Gln534His
|
|
XM_006714137.3:c.1824A>T
(F11)
|
XP_006714200.1:p.Gln608His
|
|
NM_000128.4:c.1869A>T
(F11)
MANE Select
|
NP_000119.1:p.Gln623His
|
|