ENST00000403665.7:c.*241G>A
(F11)
MANE Select
|
ENSP00000384957.2:n.*241G>A
|
|
NM_000128.3:c.*241G>A , LRG_583t1:c.*241G>A
(F11)
|
NP_000119.1:n.*241G>A
|
|
NR_033900.1:n.639C>T
(F11-AS1)
|
|
|
XM_005262821.2:c.*241G>A
(F11)
|
XP_005262878.1:n.*241G>A
|
|
XM_005262822.2:c.*241G>A
(F11)
|
XP_005262879.1:n.*241G>A
|
|
XM_005262823.2:c.*241G>A
(F11)
|
XP_005262880.1:n.*241G>A
|
|
XM_006714137.1:c.*241G>A
(F11)
|
XP_006714200.1:n.*241G>A
|
|
XM_005262821.4:c.*241G>A
(F11)
|
XP_005262878.1:n.*241G>A
|
|
XM_005262822.4:c.*241G>A
(F11)
|
XP_005262879.1:n.*241G>A
|
|
XM_005262823.4:c.*241G>A
(F11)
|
XP_005262880.1:n.*241G>A
|
|
XM_006714137.3:c.*241G>A
(F11)
|
XP_006714200.1:n.*241G>A
|
|
NM_000128.4:c.*241G>A
(F11)
MANE Select
|
NP_000119.1:n.*241G>A
|
|