ENST00000325888.13:c.7657C>G
(FLNC)
MANE Select
|
ENSP00000327145.8:p.Arg2553Gly
|
|
ENST00000325888.12:c.7657C>G
(FLNC)
|
ENSP00000327145.8:p.Arg2553Gly
|
|
ENST00000346177.6:c.7558C>G
(FLNC)
|
ENSP00000344002.6:p.Arg2520Gly
|
|
NM_001127487.1:c.7558C>G
(FLNC)
|
NP_001120959.1:p.Arg2520Gly
|
|
NM_001458.4:c.7657C>G , LRG_870t1:c.7657C>G
(FLNC)
|
NP_001449.3:p.Arg2553Gly
|
|
NR_149055.1:n.103-3816G>C
(FLNC-AS1)
|
|
|
NM_001127487.2:c.7558C>G
(FLNC)
|
NP_001120959.1:p.Arg2520Gly
|
|
NM_001458.5:c.7657C>G
(FLNC)
MANE Select
|
NP_001449.3:p.Arg2553Gly
|
|