ENST00000403665.7:c.1589A>C
(F11)
MANE Select
|
ENSP00000384957.2:p.Asn530Thr
|
|
ENST00000264691.4:c.189A>C
(F11)
|
|
|
ENST00000264692.8:c.1427A>C
(F11)
|
ENSP00000264692.5:p.Asn476Thr
|
|
ENST00000403665.6:c.1589A>C
(F11)
|
ENSP00000384957.2:p.Asn530Thr
|
|
ENST00000503841.1:n.108A>C
(F11)
|
|
|
NM_000128.3:c.1589A>C , LRG_583t1:c.1589A>C
(F11)
|
NP_000119.1:p.Asn530Thr
|
|
NR_033900.1:n.1066+732T>G
(F11-AS1)
|
|
|
XM_005262821.2:c.1592A>C
(F11)
|
XP_005262878.1:p.Asn531Thr
|
|
XM_005262822.2:c.1496A>C
(F11)
|
XP_005262879.1:p.Asn499Thr
|
|
XM_005262823.2:c.1322A>C
(F11)
|
XP_005262880.1:p.Asn441Thr
|
|
XM_006714137.1:c.1544A>C
(F11)
|
XP_006714200.1:p.Asn515Thr
|
|
XR_938706.1:n.1997A>C
(F11)
|
|
|
XR_938707.1:n.1901A>C
(F11)
|
|
|
XM_005262821.4:c.1592A>C
(F11)
|
XP_005262878.1:p.Asn531Thr
|
|
XM_005262822.4:c.1496A>C
(F11)
|
XP_005262879.1:p.Asn499Thr
|
|
XM_005262823.4:c.1322A>C
(F11)
|
XP_005262880.1:p.Asn441Thr
|
|
XM_006714137.3:c.1544A>C
(F11)
|
XP_006714200.1:p.Asn515Thr
|
|
NM_000128.4:c.1589A>C
(F11)
MANE Select
|
NP_000119.1:p.Asn530Thr
|
|