ENST00000398603.6:c.325del
|
ENSP00000381604.1:p.Tyr109ThrfsTer17
|
|
ENST00000398606.10:c.325del
MANE Select
|
ENSP00000381607.3:p.Tyr109ThrfsTer12
|
|
ENST00000646888.1:c.*41del
|
ENSP00000494477.1:n.*41del
|
|
ENST00000398603.5:c.325del
|
ENSP00000381604.1:p.Tyr109ThrfsTer17
|
|
ENST00000398606.7:c.325del
|
ENSP00000381607.3:p.Tyr109ThrfsTer12
|
|
ENST00000467591.1:n.436del
|
|
|
ENST00000494593.1:n.1120del
|
|
|
ENST00000498765.5:c.388del
|
|
|
NM_000852.3:c.325del , LRG_723t1:c.325del
|
NP_000843.1:p.Tyr109ThrfsTer12
|
|
NM_000852.4:c.325del
MANE Select
|
NP_000843.1:p.Tyr109ThrfsTer12
|
|