ENST00000325888.13:c.8165T>A
(FLNC)
MANE Select
|
ENSP00000327145.8:p.Val2722Asp
|
|
ENST00000325888.12:c.8165T>A
(FLNC)
|
ENSP00000327145.8:p.Val2722Asp
|
|
ENST00000346177.6:c.8066T>A
(FLNC)
|
ENSP00000344002.6:p.Val2689Asp
|
|
NM_001127487.1:c.8066T>A
(FLNC)
|
NP_001120959.1:p.Val2689Asp
|
|
NM_001458.4:c.8165T>A , LRG_870t1:c.8165T>A
(FLNC)
|
NP_001449.3:p.Val2722Asp
|
|
NR_149055.1:n.102+4015A>T
(FLNC-AS1)
|
|
|
NM_001127487.2:c.8066T>A
(FLNC)
|
NP_001120959.1:p.Val2689Asp
|
|
NM_001458.5:c.8165T>A
(FLNC)
MANE Select
|
NP_001449.3:p.Val2722Asp
|
|