ENST00000376335.8:c.1243del
MANE Select
|
ENSP00000365514.3:p.His415MetfsTer?
|
|
ENST00000376335.7:c.1243del
|
ENSP00000365514.3:p.His415MetfsTer?
|
|
ENST00000468291.1:n.217del
|
|
|
ENST00000477213.1:n.325del
|
|
|
ENST00000490085.5:n.289del
|
|
|
ENST00000620342.1:c.1240del
|
ENSP00000481510.1:p.His414MetfsTer?
|
|
NM_007129.3:c.1243del
|
NP_009060.2:p.His415MetfsTer?
|
|
XM_011521110.1:c.1280del
|
XP_011519412.1:p.Pro427HisfsTer?
|
|
NM_007129.4:c.1243del
|
NP_009060.2:p.His415MetfsTer?
|
|
NM_007129.5:c.1243del
MANE Select
|
NP_009060.2:p.His415MetfsTer?
|
|