ENST00000403665.7:c.1823A>G
(F11)
MANE Select
|
ENSP00000384957.2:p.Tyr608Cys
|
|
ENST00000264691.4:c.423A>G
(F11)
|
|
|
ENST00000264692.8:c.1661A>G
(F11)
|
ENSP00000264692.5:p.Tyr554Cys
|
|
ENST00000403665.6:c.1823A>G
(F11)
|
ENSP00000384957.2:p.Tyr608Cys
|
|
ENST00000503841.1:n.342A>G
(F11)
|
|
|
NM_000128.3:c.1823A>G , LRG_583t1:c.1823A>G
(F11)
|
NP_000119.1:p.Tyr608Cys
|
|
NR_033900.1:n.935T>C
(F11-AS1)
|
|
|
XM_005262821.2:c.1826A>G
(F11)
|
XP_005262878.1:p.Tyr609Cys
|
|
XM_005262822.2:c.1730A>G
(F11)
|
XP_005262879.1:p.Tyr577Cys
|
|
XM_005262823.2:c.1556A>G
(F11)
|
XP_005262880.1:p.Tyr519Cys
|
|
XM_006714137.1:c.1778A>G
(F11)
|
XP_006714200.1:p.Tyr593Cys
|
|
XM_005262821.4:c.1826A>G
(F11)
|
XP_005262878.1:p.Tyr609Cys
|
|
XM_005262822.4:c.1730A>G
(F11)
|
XP_005262879.1:p.Tyr577Cys
|
|
XM_005262823.4:c.1556A>G
(F11)
|
XP_005262880.1:p.Tyr519Cys
|
|
XM_006714137.3:c.1778A>G
(F11)
|
XP_006714200.1:p.Tyr593Cys
|
|
NM_000128.4:c.1823A>G
(F11)
MANE Select
|
NP_000119.1:p.Tyr608Cys
|
|