|
ENST00000403665.7:c.1683_1684delinsCG
(F11)
MANE Select
|
ENSP00000384957.2:p.Ala561=
|
|
|
ENST00000264691.4:c.283_284delinsCG
(F11)
|
|
|
|
ENST00000264692.8:c.1521_1522delinsCG
(F11)
|
ENSP00000264692.5:p.Ala507=
|
|
|
ENST00000403665.6:c.1683_1684delinsCG
(F11)
|
ENSP00000384957.2:p.Ala561=
|
|
|
ENST00000503841.1:n.202_203delinsCG
(F11)
|
|
|
|
NM_000128.3:c.1683_1684delinsCG , LRG_583t1:c.1683_1684delinsCG
(F11)
|
NP_000119.1:p.Ala561=
|
|
|
NR_033900.1:n.1066+637_1066+638delinsCG
(F11-AS1)
|
|
|
|
XM_005262821.2:c.1686_1687delinsCG
(F11)
|
XP_005262878.1:p.Ala562=
|
|
|
XM_005262822.2:c.1590_1591delinsCG
(F11)
|
XP_005262879.1:p.Ala530=
|
|
|
XM_005262823.2:c.1416_1417delinsCG
(F11)
|
XP_005262880.1:p.Ala472=
|
|
|
XM_006714137.1:c.1638_1639delinsCG
(F11)
|
XP_006714200.1:p.Ala546=
|
|
|
XM_005262821.4:c.1686_1687delinsCG
(F11)
|
XP_005262878.1:p.Ala562=
|
|
|
XM_005262822.4:c.1590_1591delinsCG
(F11)
|
XP_005262879.1:p.Ala530=
|
|
|
XM_005262823.4:c.1416_1417delinsCG
(F11)
|
XP_005262880.1:p.Ala472=
|
|
|
XM_006714137.3:c.1638_1639delinsCG
(F11)
|
XP_006714200.1:p.Ala546=
|
|
|
NM_000128.4:c.1683_1684delinsCG
(F11)
MANE Select
|
NP_000119.1:p.Ala561=
|
|
