ENST00000325888.13:c.7780+114_7780+115insTTAATGATACGGCG
(FLNC)
MANE Select
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ENSP00000327145.8:n.7780+114_7780+115insTTAATGATACGGCG
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ENST00000325888.12:c.7780+114_7780+115insTTAATGATACGGCG
(FLNC)
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ENSP00000327145.8:n.7780+114_7780+115insTTAATGATACGGCG
|
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ENST00000346177.6:c.7681+114_7681+115insTTAATGATACGGCG
(FLNC)
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ENSP00000344002.6:n.7681+114_7681+115insTTAATGATACGGCG
|
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NM_001127487.1:c.7681+114_7681+115insTTAATGATACGGCG
(FLNC)
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NP_001120959.1:n.7681+114_7681+115insTTAATGATACGGCG
|
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NM_001458.4:c.7780+114_7780+115insTTAATGATACGGCG , LRG_870t1:c.7780+114_7780+115insTTAATGATACGGCG
(FLNC)
|
NP_001449.3:n.7780+114_7780+115insTTAATGATACGGCG
|
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NR_149055.1:n.103-4054_103-4053insCGCCGTATCATTAA
(FLNC-AS1)
|
|
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NM_001127487.2:c.7681+114_7681+115insTTAATGATACGGCG
(FLNC)
|
NP_001120959.1:n.7681+114_7681+115insTTAATGATACGGCG
|
|
NM_001458.5:c.7780+114_7780+115insTTAATGATACGGCG
(FLNC)
MANE Select
|
NP_001449.3:n.7780+114_7780+115insTTAATGATACGGCG
|
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