ENST00000559133.6:c.4011del
|
ENSP00000453958.2:p.Val1338TyrfsTer?
|
|
ENST00000674301.2:c.4011del
|
ENSP00000501333.2:p.Val1338TyrfsTer?
|
|
ENST00000684448.1:n.2685del
|
|
|
ENST00000316623.10:c.4011del
MANE Select
|
ENSP00000325527.5:p.Val1338TyrfsTer?
|
|
ENST00000316623.9:c.4011del
|
ENSP00000325527.5:p.Val1338TyrfsTer?
|
|
ENST00000537463.6:c.683del
|
ENSP00000440294.2:p.Leu228ArgfsTer12
|
|
NM_000138.4:c.4011del , LRG_778t1:c.4011del
|
NP_000129.3:p.Val1338TyrfsTer?
|
|
NM_000138.5:c.4011del
MANE Select
|
NP_000129.3:p.Val1338TyrfsTer?
|
|