ENST00000593677.2:c.1293del
|
|
|
ENST00000688602.1:c.2690del
|
|
|
ENST00000689936.1:c.2662del
|
|
|
ENST00000359596.8:c.14357del
MANE Select
|
ENSP00000352608.2:p.Thr4786LysfsTer13
|
|
ENST00000355481.8:c.14342del
|
ENSP00000347667.3:p.Thr4781LysfsTer13
|
|
ENST00000359596.7:c.14357del
|
ENSP00000352608.2:p.Thr4786LysfsTer13
|
|
ENST00000360985.7:c.14339del
|
ENSP00000354254.4:p.Thr4780LysfsTer13
|
|
NM_000540.2:c.14357del , LRG_766t1:c.14357del
|
NP_000531.2:p.Thr4786LysfsTer13
|
|
NM_001042723.1:c.14342del
|
NP_001036188.1:p.Thr4781LysfsTer13
|
|
XM_006723317.1:c.14339del
|
XP_006723380.1:p.Thr4780LysfsTer13
|
|
XM_006723319.1:c.14324del
|
XP_006723382.1:p.Thr4775LysfsTer13
|
|
XM_011527204.1:c.14354del
|
XP_011525506.1:p.Thr4785LysfsTer13
|
|
XM_011527205.1:c.14270del
|
XP_011525507.1:p.Thr4757LysfsTer13
|
|
XM_006723317.2:c.14339del
|
XP_006723380.1:p.Thr4780LysfsTer13
|
|
XM_006723319.2:c.14324del
|
XP_006723382.1:p.Thr4775LysfsTer13
|
|
XM_011527205.2:c.14270del
|
XP_011525507.1:p.Thr4757LysfsTer13
|
|
NM_000540.3:c.14357del
MANE Select
|
NP_000531.2:p.Thr4786LysfsTer13
|
|
NM_001042723.2:c.14342del
|
NP_001036188.1:p.Thr4781LysfsTer13
|
|