ENST00000403665.7:c.1488A>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Gln496His
|
|
ENST00000264691.4:c.176+609A>C
(F11)
|
|
|
ENST00000264692.8:c.1326A>C
(F11)
|
ENSP00000264692.5:p.Gln442His
|
|
ENST00000403665.6:c.1488A>C
(F11)
|
ENSP00000384957.2:p.Gln496His
|
|
NM_000128.3:c.1488A>C , LRG_583t1:c.1488A>C
(F11)
|
NP_000119.1:p.Gln496His
|
|
NR_033900.1:n.1067-156T>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1491A>C
(F11)
|
XP_005262878.1:p.Gln497His
|
|
XM_005262822.2:c.1483+609A>C
(F11)
|
XP_005262879.1:n.1483+609A>C
|
|
XM_005262823.2:c.1221A>C
(F11)
|
XP_005262880.1:p.Gln407His
|
|
XM_005262824.1:c.1484-124A>C
(F11)
|
XP_005262881.1:n.1484-124A>C
|
|
XM_006714137.1:c.1443A>C
(F11)
|
XP_006714200.1:p.Gln481His
|
|
XR_938706.1:n.1896A>C
(F11)
|
|
|
XR_938707.1:n.1888+609A>C
(F11)
|
|
|
XM_005262821.4:c.1491A>C
(F11)
|
XP_005262878.1:p.Gln497His
|
|
XM_005262822.4:c.1483+609A>C
(F11)
|
XP_005262879.1:n.1483+609A>C
|
|
XM_005262823.4:c.1221A>C
(F11)
|
XP_005262880.1:p.Gln407His
|
|
XM_006714137.3:c.1443A>C
(F11)
|
XP_006714200.1:p.Gln481His
|
|
XR_001741172.2:n.1962A>C
(F11)
|
|
|
NM_000128.4:c.1488A>C
(F11)
MANE Select
|
NP_000119.1:p.Gln496His
|
|