ENST00000403665.7:c.1492C>G
(F11)
MANE Select
|
ENSP00000384957.2:p.Pro498Ala
|
|
ENST00000264691.4:c.176+613C>G
(F11)
|
|
|
ENST00000264692.8:c.1330C>G
(F11)
|
ENSP00000264692.5:p.Pro444Ala
|
|
ENST00000403665.6:c.1492C>G
(F11)
|
ENSP00000384957.2:p.Pro498Ala
|
|
NM_000128.3:c.1492C>G , LRG_583t1:c.1492C>G
(F11)
|
NP_000119.1:p.Pro498Ala
|
|
NR_033900.1:n.1067-160G>C
(F11-AS1)
|
|
|
XM_005262821.2:c.1495C>G
(F11)
|
XP_005262878.1:p.Pro499Ala
|
|
XM_005262822.2:c.1483+613C>G
(F11)
|
XP_005262879.1:n.1483+613C>G
|
|
XM_005262823.2:c.1225C>G
(F11)
|
XP_005262880.1:p.Pro409Ala
|
|
XM_005262824.1:c.1484-120C>G
(F11)
|
XP_005262881.1:n.1484-120C>G
|
|
XM_006714137.1:c.1447C>G
(F11)
|
XP_006714200.1:p.Pro483Ala
|
|
XR_938706.1:n.1900C>G
(F11)
|
|
|
XR_938707.1:n.1888+613C>G
(F11)
|
|
|
XM_005262821.4:c.1495C>G
(F11)
|
XP_005262878.1:p.Pro499Ala
|
|
XM_005262822.4:c.1483+613C>G
(F11)
|
XP_005262879.1:n.1483+613C>G
|
|
XM_005262823.4:c.1225C>G
(F11)
|
XP_005262880.1:p.Pro409Ala
|
|
XM_006714137.3:c.1447C>G
(F11)
|
XP_006714200.1:p.Pro483Ala
|
|
XR_001741172.2:n.1966C>G
(F11)
|
|
|
NM_000128.4:c.1492C>G
(F11)
MANE Select
|
NP_000119.1:p.Pro498Ala
|
|