|
NM_032199.3:c.1302del
MANE Select
|
NP_115575.1:p.Asn434LysfsTer?
|
|
ENST00000279873.12:c.1302del
MANE Select
|
ENSP00000279873.7:p.Asn434LysfsTer?
|
|
NM_001244638.1:c.573del
|
NP_001231567.1:p.Asn191LysfsTer?
|
|
NM_001244638.2:c.573del
|
NP_001231567.1:p.Asn191LysfsTer?
|
|
NM_032199.2:c.1302del
|
NP_115575.1:p.Asn434LysfsTer?
|
|
ENST00000279873.11:c.1302del
|
ENSP00000279873.7:p.Asn434LysfsTer?
|
|
ENST00000309334.5:c.573del
|
ENSP00000308862.5:p.Asn191LysfsTer?
|
|
ENST00000681100.1:c.1278del
|
ENSP00000506119.1:p.Asn426LysfsTer?
|
|
XM_011540262.1:c.1071del
|
XP_011538564.1:p.Asn357LysfsTer?
|
|
XM_024448230.1:c.735del
|
XP_024303998.1:p.Asn245LysfsTer?
|
|
XM_024448231.1:c.-175del
|
XP_024303999.1:n.-175del
|