ENST00000398603.6:c.337-216C>A
|
ENSP00000381604.1:n.337-216C>A
|
|
ENST00000398606.10:c.406C>A
MANE Select
|
ENSP00000381607.3:p.Gln136Lys
|
|
ENST00000646888.1:c.*122C>A
|
ENSP00000494477.1:n.*122C>A
|
|
ENST00000398603.5:c.337-216C>A
|
ENSP00000381604.1:n.337-216C>A
|
|
ENST00000398606.7:c.406C>A
|
ENSP00000381607.3:p.Gln136Lys
|
|
ENST00000467591.1:n.517C>A
|
|
|
ENST00000494593.1:n.1201C>A
|
|
|
ENST00000495996.1:c.70C>A
|
ENSP00000484686.1:p.Gln24Lys
|
|
ENST00000498765.5:c.469C>A
|
|
|
NM_000852.3:c.406C>A , LRG_723t1:c.406C>A
|
NP_000843.1:p.Gln136Lys
|
|
NM_000852.4:c.406C>A
MANE Select
|
NP_000843.1:p.Gln136Lys
|
|