ENST00000403665.7:c.1550C>G
(F11)
MANE Select
|
ENSP00000384957.2:p.Thr517Ser
|
|
ENST00000264691.4:c.176+671C>G
(F11)
|
|
|
ENST00000264692.8:c.1388C>G
(F11)
|
ENSP00000264692.5:p.Thr463Ser
|
|
ENST00000403665.6:c.1550C>G
(F11)
|
ENSP00000384957.2:p.Thr517Ser
|
|
NM_000128.3:c.1550C>G , LRG_583t1:c.1550C>G
(F11)
|
NP_000119.1:p.Thr517Ser
|
|
NR_033900.1:n.1067-218G>C
(F11-AS1)
|
|
|
XM_005262821.2:c.1553C>G
(F11)
|
XP_005262878.1:p.Thr518Ser
|
|
XM_005262822.2:c.1483+671C>G
(F11)
|
XP_005262879.1:n.1483+671C>G
|
|
XM_005262823.2:c.1283C>G
(F11)
|
XP_005262880.1:p.Thr428Ser
|
|
XM_005262824.1:c.1484-62C>G
(F11)
|
XP_005262881.1:n.1484-62C>G
|
|
XM_006714137.1:c.1505C>G
(F11)
|
XP_006714200.1:p.Thr502Ser
|
|
XR_938706.1:n.1958C>G
(F11)
|
|
|
XR_938707.1:n.1888+671C>G
(F11)
|
|
|
XM_005262821.4:c.1553C>G
(F11)
|
XP_005262878.1:p.Thr518Ser
|
|
XM_005262822.4:c.1483+671C>G
(F11)
|
XP_005262879.1:n.1483+671C>G
|
|
XM_005262823.4:c.1283C>G
(F11)
|
XP_005262880.1:p.Thr428Ser
|
|
XM_006714137.3:c.1505C>G
(F11)
|
XP_006714200.1:p.Thr502Ser
|
|
XR_001741172.2:n.2024C>G
(F11)
|
|
|
NM_000128.4:c.1550C>G
(F11)
MANE Select
|
NP_000119.1:p.Thr517Ser
|
|