ENST00000398603.6:c.486_487del
|
ENSP00000381604.1:p.Tyr163ArgfsTer?
|
|
ENST00000398606.10:c.594_595del
MANE Select
|
ENSP00000381607.3:p.Tyr199ArgfsTer?
|
|
ENST00000398603.5:c.486_487del
|
ENSP00000381604.1:p.Tyr163ArgfsTer?
|
|
ENST00000398606.7:c.594_595del
|
ENSP00000381607.3:p.Tyr199ArgfsTer?
|
|
ENST00000467591.1:n.705_706del
|
|
|
ENST00000494593.1:n.1566_1567del
|
|
|
ENST00000498765.5:c.657_658del
|
|
|
NM_000852.3:c.594_595del , LRG_723t1:c.594_595del
|
NP_000843.1:p.Tyr199ArgfsTer?
|
|
NM_000852.4:c.594_595del
MANE Select
|
NP_000843.1:p.Tyr199ArgfsTer?
|
|