ENST00000403665.7:c.1603G>A
(F11)
MANE Select
|
ENSP00000384957.2:p.Ala535Thr
|
|
ENST00000264691.4:c.203G>A
(F11)
|
|
|
ENST00000264692.8:c.1441G>A
(F11)
|
ENSP00000264692.5:p.Ala481Thr
|
|
ENST00000403665.6:c.1603G>A
(F11)
|
ENSP00000384957.2:p.Ala535Thr
|
|
ENST00000503841.1:n.122G>A
(F11)
|
|
|
NM_000128.3:c.1603G>A , LRG_583t1:c.1603G>A
(F11)
|
NP_000119.1:p.Ala535Thr
|
|
NR_033900.1:n.1066+718C>T
(F11-AS1)
|
|
|
XM_005262821.2:c.1606G>A
(F11)
|
XP_005262878.1:p.Ala536Thr
|
|
XM_005262822.2:c.1510G>A
(F11)
|
XP_005262879.1:p.Ala504Thr
|
|
XM_005262823.2:c.1336G>A
(F11)
|
XP_005262880.1:p.Ala446Thr
|
|
XM_006714137.1:c.1558G>A
(F11)
|
XP_006714200.1:p.Ala520Thr
|
|
XR_938707.1:n.1915G>A
(F11)
|
|
|
XM_005262821.4:c.1606G>A
(F11)
|
XP_005262878.1:p.Ala536Thr
|
|
XM_005262822.4:c.1510G>A
(F11)
|
XP_005262879.1:p.Ala504Thr
|
|
XM_005262823.4:c.1336G>A
(F11)
|
XP_005262880.1:p.Ala446Thr
|
|
XM_006714137.3:c.1558G>A
(F11)
|
XP_006714200.1:p.Ala520Thr
|
|
NM_000128.4:c.1603G>A
(F11)
MANE Select
|
NP_000119.1:p.Ala535Thr
|
|