ENST00000403665.7:c.1772G=
(F11)
MANE Select
|
ENSP00000384957.2:p.Gly591=
|
|
ENST00000264691.4:c.372G=
(F11)
|
|
|
ENST00000264692.8:c.1610G=
(F11)
|
ENSP00000264692.5:p.Gly537=
|
|
ENST00000403665.6:c.1772G=
(F11)
|
ENSP00000384957.2:p.Gly591=
|
|
ENST00000503841.1:n.291G=
(F11)
|
|
|
NM_000128.3:c.1772G= , LRG_583t1:c.1772G=
(F11)
|
NP_000119.1:p.Gly591=
|
|
NR_033900.1:n.986C=
(F11-AS1)
|
|
|
XM_005262821.2:c.1775G=
(F11)
|
XP_005262878.1:p.Gly592=
|
|
XM_005262822.2:c.1679G=
(F11)
|
XP_005262879.1:p.Gly560=
|
|
XM_005262823.2:c.1505G=
(F11)
|
XP_005262880.1:p.Gly502=
|
|
XM_006714137.1:c.1727G=
(F11)
|
XP_006714200.1:p.Gly576=
|
|
XM_005262821.4:c.1775G=
(F11)
|
XP_005262878.1:p.Gly592=
|
|
XM_005262822.4:c.1679G=
(F11)
|
XP_005262879.1:p.Gly560=
|
|
XM_005262823.4:c.1505G=
(F11)
|
XP_005262880.1:p.Gly502=
|
|
XM_006714137.3:c.1727G=
(F11)
|
XP_006714200.1:p.Gly576=
|
|
NM_000128.4:c.1772G=
(F11)
MANE Select
|
NP_000119.1:p.Gly591=
|
|