ENST00000403665.7:c.1687T>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Tyr563His
|
|
ENST00000264691.4:c.287T>C
(F11)
|
|
|
ENST00000264692.8:c.1525T>C
(F11)
|
ENSP00000264692.5:p.Tyr509His
|
|
ENST00000403665.6:c.1687T>C
(F11)
|
ENSP00000384957.2:p.Tyr563His
|
|
ENST00000503841.1:n.206T>C
(F11)
|
|
|
NM_000128.3:c.1687T>C , LRG_583t1:c.1687T>C
(F11)
|
NP_000119.1:p.Tyr563His
|
|
NR_033900.1:n.1066+634A>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1690T>C
(F11)
|
XP_005262878.1:p.Tyr564His
|
|
XM_005262822.2:c.1594T>C
(F11)
|
XP_005262879.1:p.Tyr532His
|
|
XM_005262823.2:c.1420T>C
(F11)
|
XP_005262880.1:p.Tyr474His
|
|
XM_006714137.1:c.1642T>C
(F11)
|
XP_006714200.1:p.Tyr548His
|
|
XM_005262821.4:c.1690T>C
(F11)
|
XP_005262878.1:p.Tyr564His
|
|
XM_005262822.4:c.1594T>C
(F11)
|
XP_005262879.1:p.Tyr532His
|
|
XM_005262823.4:c.1420T>C
(F11)
|
XP_005262880.1:p.Tyr474His
|
|
XM_006714137.3:c.1642T>C
(F11)
|
XP_006714200.1:p.Tyr548His
|
|
NM_000128.4:c.1687T>C
(F11)
MANE Select
|
NP_000119.1:p.Tyr563His
|
|