ENST00000325888.13:c.5633C>T
(FLNC)
MANE Select
|
ENSP00000327145.8:p.Ala1878Val
|
|
ENST00000325888.12:c.5633C>T
(FLNC)
|
ENSP00000327145.8:p.Ala1878Val
|
|
ENST00000346177.6:c.5534C>T
(FLNC)
|
ENSP00000344002.6:p.Ala1845Val
|
|
NM_001127487.1:c.5534C>T
(FLNC)
|
NP_001120959.1:p.Ala1845Val
|
|
NM_001458.4:c.5633C>T , LRG_870t1:c.5633C>T
(FLNC)
|
NP_001449.3:p.Ala1878Val
|
|
NR_149055.1:n.315+76G>A
(FLNC-AS1)
|
|
|
NM_001127487.2:c.5534C>T
(FLNC)
|
NP_001120959.1:p.Ala1845Val
|
|
NM_001458.5:c.5633C>T
(FLNC)
MANE Select
|
NP_001449.3:p.Ala1878Val
|
|