ENST00000355832.10:c.3562_3565delinsCATA
MANE Select
|
ENSP00000348089.5:p.His1188=
|
|
ENST00000679552.1:n.633_636delinsCATA
|
|
|
ENST00000679871.1:n.708_711delinsCATA
|
|
|
ENST00000679974.1:n.611_614delinsCATA
|
|
|
ENST00000681632.1:n.4965_4968delinsCATA
|
|
|
ENST00000681659.1:c.3403_3406delinsCATA
|
ENSP00000505631.1:p.His1135=
|
|
ENST00000355832.9:c.3562_3565delinsCATA
|
ENSP00000348089.5:p.His1188=
|
|
ENST00000623073.3:c.*1858_*1861delinsCATA
|
ENSP00000485650.1:n.*1858_*1861delinsCATA
|
|
ENST00000623115.3:c.1672_1675delinsCATA
|
ENSP00000485321.1:p.His558=
|
|
ENST00000624341.3:c.1394_1397delinsCATA
|
|
|
NM_000124.3:c.3562_3565delinsCATA
|
NP_000115.1:p.His1188=
|
|
XR_945953.1:n.243-1170_243-1167delinsTATG
|
|
|
NM_001346440.1:c.3562_3565delinsCATA
|
NP_001333369.1:p.His1188=
|
|
NM_000124.4:c.3562_3565delinsCATA
MANE Select
|
NP_000115.1:p.His1188=
|
|
NM_001346440.2:c.3562_3565delinsCATA
|
NP_001333369.1:p.His1188=
|
|