ENST00000674537.2:c.2176C>A
|
ENSP00000502725.1:p.Gln726Lys
|
|
ENST00000392302.7:c.2176C>A
|
ENSP00000376120.3:p.Gln726Lys
|
|
ENST00000497019.7:c.*948C>A
|
ENSP00000436804.2:n.*948C>A
|
|
ENST00000524377.7:c.2356C>A
MANE Select
|
ENSP00000431418.1:p.Gln786Lys
|
|
ENST00000531606.2:c.415C>A
|
|
|
ENST00000674537.1:c.2176C>A
|
ENSP00000502725.1:p.Gln726Lys
|
|
ENST00000358660.3:c.2347C>A
|
ENSP00000351486.3:p.Gln783Lys
|
|
ENST00000368196.7:c.2338C>A
|
ENSP00000357179.3:p.Gln780Lys
|
|
ENST00000392302.6:c.2248C>A
|
ENSP00000376120.2:p.Gln750Lys
|
|
ENST00000497019.6:c.*948C>A
|
ENSP00000436804.1:n.*948C>A
|
|
ENST00000524377.5:c.2356C>A
|
ENSP00000431418.1:p.Gln786Lys
|
|
ENST00000530298.5:n.2809C>A
|
|
|
ENST00000531606.1:n.399C>A
|
|
|
NM_001007792.1:c.2248C>A , LRG_261t1:c.2248C>A
|
NP_001007793.1:p.Gln750Lys
|
|
NM_001012331.1:c.2338C>A , LRG_261t2:c.2338C>A
|
NP_001012331.1:p.Gln780Lys
|
|
NM_002529.3:c.2356C>A , LRG_261t3:c.2356C>A
|
NP_002520.2:p.Gln786Lys
|
|
NM_001012331.2:c.2338C>A
|
NP_001012331.1:p.Gln780Lys
|
|
NM_002529.4:c.2356C>A
MANE Select
|
NP_002520.2:p.Gln786Lys
|
|