ENST00000325888.13:c.8074T>G
(FLNC)
MANE Select
|
ENSP00000327145.8:p.Tyr2692Asp
|
|
ENST00000325888.12:c.8074T>G
(FLNC)
|
ENSP00000327145.8:p.Tyr2692Asp
|
|
ENST00000346177.6:c.7975T>G
(FLNC)
|
ENSP00000344002.6:p.Tyr2659Asp
|
|
NM_001127487.1:c.7975T>G
(FLNC)
|
NP_001120959.1:p.Tyr2659Asp
|
|
NM_001458.4:c.8074T>G , LRG_870t1:c.8074T>G
(FLNC)
|
NP_001449.3:p.Tyr2692Asp
|
|
NR_149055.1:n.102+4106A>C
(FLNC-AS1)
|
|
|
NM_001127487.2:c.7975T>G
(FLNC)
|
NP_001120959.1:p.Tyr2659Asp
|
|
NM_001458.5:c.8074T>G
(FLNC)
MANE Select
|
NP_001449.3:p.Tyr2692Asp
|
|