ENST00000403665.7:c.1785_1791delinsGGGCGAA
(F11)
MANE Select
|
ENSP00000384957.2:p.Trp595=
|
|
ENST00000264691.4:c.385_391delinsGGGCGAA
(F11)
|
|
|
ENST00000264692.8:c.1623_1629delinsGGGCGAA
(F11)
|
ENSP00000264692.5:p.Trp541=
|
|
ENST00000403665.6:c.1785_1791delinsGGGCGAA
(F11)
|
ENSP00000384957.2:p.Trp595=
|
|
ENST00000503841.1:n.304_310delinsGGGCGAA
(F11)
|
|
|
NM_000128.3:c.1785_1791delinsGGGCGAA , LRG_583t1:c.1785_1791delinsGGGCGAA
(F11)
|
NP_000119.1:p.Trp595=
|
|
NR_033900.1:n.967_973delinsTTCGCCC
(F11-AS1)
|
|
|
XM_005262821.2:c.1788_1794delinsGGGCGAA
(F11)
|
XP_005262878.1:p.Trp596=
|
|
XM_005262822.2:c.1692_1698delinsGGGCGAA
(F11)
|
XP_005262879.1:p.Trp564=
|
|
XM_005262823.2:c.1518_1524delinsGGGCGAA
(F11)
|
XP_005262880.1:p.Trp506=
|
|
XM_006714137.1:c.1740_1746delinsGGGCGAA
(F11)
|
XP_006714200.1:p.Trp580=
|
|
XM_005262821.4:c.1788_1794delinsGGGCGAA
(F11)
|
XP_005262878.1:p.Trp596=
|
|
XM_005262822.4:c.1692_1698delinsGGGCGAA
(F11)
|
XP_005262879.1:p.Trp564=
|
|
XM_005262823.4:c.1518_1524delinsGGGCGAA
(F11)
|
XP_005262880.1:p.Trp506=
|
|
XM_006714137.3:c.1740_1746delinsGGGCGAA
(F11)
|
XP_006714200.1:p.Trp580=
|
|
NM_000128.4:c.1785_1791delinsGGGCGAA
(F11)
MANE Select
|
NP_000119.1:p.Trp595=
|
|