ENST00000398603.6:c.377T>A
|
ENSP00000381604.1:p.Ile126Asn
|
|
ENST00000398606.10:c.485T>A
MANE Select
|
ENSP00000381607.3:p.Ile162Asn
|
|
ENST00000646888.1:c.*201T>A
|
ENSP00000494477.1:n.*201T>A
|
|
ENST00000398603.5:c.377T>A
|
ENSP00000381604.1:p.Ile126Asn
|
|
ENST00000398606.7:c.485T>A
|
ENSP00000381607.3:p.Ile162Asn
|
|
ENST00000467591.1:n.596T>A
|
|
|
ENST00000494593.1:n.1457T>A
|
|
|
ENST00000495996.1:c.211T>A
|
ENSP00000484686.1:n.211T>A
|
|
ENST00000498765.5:c.548T>A
|
|
|
NM_000852.3:c.485T>A , LRG_723t1:c.485T>A
|
NP_000843.1:p.Ile162Asn
|
|
NM_000852.4:c.485T>A
MANE Select
|
NP_000843.1:p.Ile162Asn
|
|