ENST00000586171.3:c.1001_1013del
|
ENSP00000467120.2:p.Ile334LysfsTer?
|
|
ENST00000700232.1:c.1001_1013del
|
ENSP00000514870.1:p.Ile334LysfsTer?
|
|
ENST00000292431.5:c.1001_1013del
MANE Select
|
ENSP00000292431.3:p.Ile334LysfsTer?
|
|
ENST00000292431.4:c.1001_1013del
|
ENSP00000292431.3:p.Ile334LysfsTer?
|
|
NM_052876.3:c.1001_1013del
|
NP_443108.1:p.Ile334LysfsTer?
|
|
XM_005259721.2:c.1001_1013del
|
XP_005259778.1:p.Ile334LysfsTer?
|
|
XM_005259721.3:c.1001_1013del
|
XP_005259778.1:p.Ile334LysfsTer?
|
|
NM_052876.4:c.1001_1013del
MANE Select
|
NP_443108.1:p.Ile334LysfsTer?
|
|