ENST00000398603.6:c.293_294insTTTTTTTAAT
|
ENSP00000381604.1:p.Glu98AspfsTer23
|
|
ENST00000398606.10:c.293_294insTTTTTTTAAT
MANE Select
|
ENSP00000381607.3:p.Glu98AspfsTer19
|
|
ENST00000646888.1:c.*9_*10insTTTTTTTAAT
|
ENSP00000494477.1:n.*9_*10insTTTTTTTAAT
|
|
ENST00000398603.5:c.293_294insTTTTTTTAAT
|
ENSP00000381604.1:p.Glu98AspfsTer23
|
|
ENST00000398606.7:c.293_294insTTTTTTTAAT
|
ENSP00000381607.3:p.Glu98AspfsTer19
|
|
ENST00000467591.1:n.404_405insTTTTTTTAAT
|
|
|
ENST00000494593.1:n.1088_1089insTTTTTTTAAT
|
|
|
ENST00000498765.5:c.356_357insTTTTTTTAAT
|
|
|
NM_000852.3:c.293_294insTTTTTTTAAT , LRG_723t1:c.293_294insTTTTTTTAAT
|
NP_000843.1:p.Glu98AspfsTer19
|
|
NM_000852.4:c.293_294insTTTTTTTAAT
MANE Select
|
NP_000843.1:p.Glu98AspfsTer19
|
|