ENST00000403665.7:c.1628A>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Glu543Ala
|
|
ENST00000264691.4:c.228A>C
(F11)
|
|
|
ENST00000264692.8:c.1466A>C
(F11)
|
ENSP00000264692.5:p.Glu489Ala
|
|
ENST00000403665.6:c.1628A>C
(F11)
|
ENSP00000384957.2:p.Glu543Ala
|
|
ENST00000503841.1:n.147A>C
(F11)
|
|
|
NM_000128.3:c.1628A>C , LRG_583t1:c.1628A>C
(F11)
|
NP_000119.1:p.Glu543Ala
|
|
NR_033900.1:n.1066+693T>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1631A>C
(F11)
|
XP_005262878.1:p.Glu544Ala
|
|
XM_005262822.2:c.1535A>C
(F11)
|
XP_005262879.1:p.Glu512Ala
|
|
XM_005262823.2:c.1361A>C
(F11)
|
XP_005262880.1:p.Glu454Ala
|
|
XM_006714137.1:c.1583A>C
(F11)
|
XP_006714200.1:p.Glu528Ala
|
|
XR_938707.1:n.1940A>C
(F11)
|
|
|
XM_005262821.4:c.1631A>C
(F11)
|
XP_005262878.1:p.Glu544Ala
|
|
XM_005262822.4:c.1535A>C
(F11)
|
XP_005262879.1:p.Glu512Ala
|
|
XM_005262823.4:c.1361A>C
(F11)
|
XP_005262880.1:p.Glu454Ala
|
|
XM_006714137.3:c.1583A>C
(F11)
|
XP_006714200.1:p.Glu528Ala
|
|
NM_000128.4:c.1628A>C
(F11)
MANE Select
|
NP_000119.1:p.Glu543Ala
|
|