ENST00000403665.7:c.1627G>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Glu543Gln
|
|
ENST00000264691.4:c.227G>C
(F11)
|
|
|
ENST00000264692.8:c.1465G>C
(F11)
|
ENSP00000264692.5:p.Glu489Gln
|
|
ENST00000403665.6:c.1627G>C
(F11)
|
ENSP00000384957.2:p.Glu543Gln
|
|
ENST00000503841.1:n.146G>C
(F11)
|
|
|
NM_000128.3:c.1627G>C , LRG_583t1:c.1627G>C
(F11)
|
NP_000119.1:p.Glu543Gln
|
|
NR_033900.1:n.1066+694C>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1630G>C
(F11)
|
XP_005262878.1:p.Glu544Gln
|
|
XM_005262822.2:c.1534G>C
(F11)
|
XP_005262879.1:p.Glu512Gln
|
|
XM_005262823.2:c.1360G>C
(F11)
|
XP_005262880.1:p.Glu454Gln
|
|
XM_006714137.1:c.1582G>C
(F11)
|
XP_006714200.1:p.Glu528Gln
|
|
XR_938707.1:n.1939G>C
(F11)
|
|
|
XM_005262821.4:c.1630G>C
(F11)
|
XP_005262878.1:p.Glu544Gln
|
|
XM_005262822.4:c.1534G>C
(F11)
|
XP_005262879.1:p.Glu512Gln
|
|
XM_005262823.4:c.1360G>C
(F11)
|
XP_005262880.1:p.Glu454Gln
|
|
XM_006714137.3:c.1582G>C
(F11)
|
XP_006714200.1:p.Glu528Gln
|
|
NM_000128.4:c.1627G>C
(F11)
MANE Select
|
NP_000119.1:p.Glu543Gln
|
|