ENST00000325888.13:c.7252-29A>G
(FLNC)
MANE Select
|
ENSP00000327145.8:n.7252-29A>G
|
|
ENST00000325888.12:c.7252-29A>G
(FLNC)
|
ENSP00000327145.8:n.7252-29A>G
|
|
ENST00000346177.6:c.7153-29A>G
(FLNC)
|
ENSP00000344002.6:n.7153-29A>G
|
|
NM_001127487.1:c.7153-29A>G
(FLNC)
|
NP_001120959.1:n.7153-29A>G
|
|
NM_001458.4:c.7252-29A>G , LRG_870t1:c.7252-29A>G
(FLNC)
|
NP_001449.3:n.7252-29A>G
|
|
NR_149055.1:n.103-3092T>C
(FLNC-AS1)
|
|
|
NM_001127487.2:c.7153-29A>G
(FLNC)
|
NP_001120959.1:n.7153-29A>G
|
|
NM_001458.5:c.7252-29A>G
(FLNC)
MANE Select
|
NP_001449.3:n.7252-29A>G
|
|