ENST00000398603.6:c.337-193dup
|
ENSP00000381604.1:n.337-193dup
|
|
ENST00000398606.10:c.429dup
MANE Select
|
ENSP00000381607.3:p.Ile144HisfsTer10
|
|
ENST00000646888.1:c.*145dup
|
ENSP00000494477.1:n.*145dup
|
|
ENST00000398603.5:c.337-193dup
|
ENSP00000381604.1:n.337-193dup
|
|
ENST00000398606.7:c.429dup
|
ENSP00000381607.3:p.Ile144HisfsTer10
|
|
ENST00000467591.1:n.540dup
|
|
|
ENST00000494593.1:n.1224dup
|
|
|
ENST00000495996.1:c.93dup
|
ENSP00000484686.1:p.Ile32HisfsTer?
|
|
ENST00000498765.5:c.492dup
|
|
|
NM_000852.3:c.429dup , LRG_723t1:c.429dup
|
NP_000843.1:p.Ile144HisfsTer10
|
|
NM_000852.4:c.429dup
MANE Select
|
NP_000843.1:p.Ile144HisfsTer10
|
|