ENST00000325888.13:c.6004+29G>A
(FLNC)
MANE Select
|
ENSP00000327145.8:n.6004+29G>A
|
|
ENST00000325888.12:c.6004+29G>A
(FLNC)
|
ENSP00000327145.8:n.6004+29G>A
|
|
ENST00000346177.6:c.5905+29G>A
(FLNC)
|
ENSP00000344002.6:n.5905+29G>A
|
|
NM_001127487.1:c.5905+29G>A
(FLNC)
|
NP_001120959.1:n.5905+29G>A
|
|
NM_001458.4:c.6004+29G>A , LRG_870t1:c.6004+29G>A
(FLNC)
|
NP_001449.3:n.6004+29G>A
|
|
NR_149055.1:n.215+504C>T
(FLNC-AS1)
|
|
|
NM_001127487.2:c.5905+29G>A
(FLNC)
|
NP_001120959.1:n.5905+29G>A
|
|
NM_001458.5:c.6004+29G>A
(FLNC)
MANE Select
|
NP_001449.3:n.6004+29G>A
|
|