ENST00000325888.13:c.8006T>A
(FLNC)
MANE Select
|
ENSP00000327145.8:p.Met2669Lys
|
|
ENST00000325888.12:c.8006T>A
(FLNC)
|
ENSP00000327145.8:p.Met2669Lys
|
|
ENST00000346177.6:c.7907T>A
(FLNC)
|
ENSP00000344002.6:p.Met2636Lys
|
|
NM_001127487.1:c.7907T>A
(FLNC)
|
NP_001120959.1:p.Met2636Lys
|
|
NM_001458.4:c.8006T>A , LRG_870t1:c.8006T>A
(FLNC)
|
NP_001449.3:p.Met2669Lys
|
|
NR_149055.1:n.102+4174A>T
(FLNC-AS1)
|
|
|
NM_001127487.2:c.7907T>A
(FLNC)
|
NP_001120959.1:p.Met2636Lys
|
|
NM_001458.5:c.8006T>A
(FLNC)
MANE Select
|
NP_001449.3:p.Met2669Lys
|
|