ENST00000403665.7:c.1824C=
(F11)
MANE Select
|
ENSP00000384957.2:p.Tyr608=
|
|
ENST00000264691.4:c.424C=
(F11)
|
|
|
ENST00000264692.8:c.1662C=
(F11)
|
ENSP00000264692.5:p.Tyr554=
|
|
ENST00000403665.6:c.1824C=
(F11)
|
ENSP00000384957.2:p.Tyr608=
|
|
ENST00000503841.1:n.343C=
(F11)
|
|
|
NM_000128.3:c.1824C= , LRG_583t1:c.1824C=
(F11)
|
NP_000119.1:p.Tyr608=
|
|
NR_033900.1:n.934G=
(F11-AS1)
|
|
|
XM_005262821.2:c.1827C=
(F11)
|
XP_005262878.1:p.Tyr609=
|
|
XM_005262822.2:c.1731C=
(F11)
|
XP_005262879.1:p.Tyr577=
|
|
XM_005262823.2:c.1557C=
(F11)
|
XP_005262880.1:p.Tyr519=
|
|
XM_006714137.1:c.1779C=
(F11)
|
XP_006714200.1:p.Tyr593=
|
|
XM_005262821.4:c.1827C=
(F11)
|
XP_005262878.1:p.Tyr609=
|
|
XM_005262822.4:c.1731C=
(F11)
|
XP_005262879.1:p.Tyr577=
|
|
XM_005262823.4:c.1557C=
(F11)
|
XP_005262880.1:p.Tyr519=
|
|
XM_006714137.3:c.1779C=
(F11)
|
XP_006714200.1:p.Tyr593=
|
|
NM_000128.4:c.1824C=
(F11)
MANE Select
|
NP_000119.1:p.Tyr608=
|
|