|
NM_015346.4:c.6713T>A
MANE Select
|
NP_056161.2:p.Leu2238Ter
|
|
ENST00000347230.9:c.6713T>A
MANE Select
|
ENSP00000251119.5:p.Leu2238Ter
|
|
NM_015346.3:c.6713T>A
|
NP_056161.2:p.Leu2238Ter
|
|
ENST00000347230.8:c.6713T>A
|
ENSP00000251119.5:p.Leu2238Ter
|
|
ENST00000394455.6:n.1976T>A
|
|
|
ENST00000554523.5:n.7468T>A
|
|
|
ENST00000554557.5:c.*4691T>A
|
ENSP00000450431.1:n.*4691T>A
|
|
ENST00000554783.1:n.401T>A
|
|
|
ENST00000557306.1:c.251T>A
|
ENSP00000452142.1:p.Leu84Ter
|
|
ENST00000676512.1:c.6731T>A
|
ENSP00000504552.1:p.Leu2244Ter
|
|
ENST00000676620.1:c.6635T>A
|
ENSP00000504587.1:p.Leu2212Ter
|
|
ENST00000678386.1:c.6758T>A
|
ENSP00000503677.1:p.Leu2253Ter
|
|
XM_006720093.2:c.6713T>A
|
XP_006720156.1:p.Leu2238Ter
|
|
XM_011536606.1:c.5204T>A
|
XP_011534908.1:p.Leu1735Ter
|
|
XM_011536607.1:c.4388T>A
|
XP_011534909.1:p.Leu1463Ter
|
|
XM_011536608.1:c.4295T>A
|
XP_011534910.1:p.Leu1432Ter
|
|
XM_017021124.1:c.6731T>A
|
XP_016876613.1:p.Leu2244Ter
|
|
XM_017021125.1:c.6731T>A
|
XP_016876614.1:p.Leu2244Ter
|
|
XM_017021126.1:c.5222T>A
|
XP_016876615.1:p.Leu1741Ter
|
|
XM_017021127.2:c.4406T>A
|
XP_016876616.1:p.Leu1469Ter
|
|
XM_017021128.1:c.4313T>A
|
XP_016876617.1:p.Leu1438Ter
|