ENST00000697843.1:n.2639G>C
|
|
|
ENST00000373189.6:c.1163G>C
MANE Select
|
ENSP00000362285.5:p.Cys388Ser
|
|
ENST00000479577.2:c.929G>C
|
ENSP00000493995.1:p.Cys310Ser
|
|
ENST00000642198.1:c.*735G>C
|
ENSP00000494827.1:n.*735G>C
|
|
ENST00000642772.1:c.*94+6100G>C
|
ENSP00000495041.1:n.*94+6100G>C
|
|
ENST00000643042.1:c.784G>C
|
ENSP00000496674.1:n.784G>C
|
|
ENST00000643619.1:c.*746G>C
|
ENSP00000494378.1:n.*746G>C
|
|
ENST00000643752.1:c.*489G>C
|
ENSP00000495000.1:n.*489G>C
|
|
ENST00000644088.1:c.*484G>C
|
ENSP00000494066.1:n.*484G>C
|
|
ENST00000644591.1:c.*489G>C
|
ENSP00000496664.1:n.*489G>C
|
|
ENST00000644895.1:c.*99+6100G>C
|
ENSP00000493872.1:n.*99+6100G>C
|
|
ENST00000645345.1:c.*735G>C
|
ENSP00000495859.1:n.*735G>C
|
|
ENST00000647524.1:c.*746G>C
|
ENSP00000495077.1:n.*746G>C
|
|
ENST00000373189.5:c.1163G>C
|
ENSP00000362285.5:p.Cys388Ser
|
|
ENST00000469204.1:n.660G>C
|
|
|
NM_001174098.1:c.*392G>C
|
NP_001167569.1:n.*392G>C
|
|
NM_018344.5:c.1163G>C
|
NP_060814.4:p.Cys388Ser
|
|
NR_033413.1:n.1137G>C
|
|
|
NR_033414.1:n.910G>C
|
|
|
XM_006717910.2:c.929G>C
|
XP_006717973.1:p.Cys310Ser
|
|
NM_001363518.1:c.929G>C
|
NP_001350447.1:p.Cys310Ser
|
|
XM_017016377.2:c.725G>C
|
XP_016871866.1:p.Cys242Ser
|
|
XM_017016378.2:c.545G>C
|
XP_016871867.1:p.Cys182Ser
|
|
NM_018344.6:c.1163G>C
MANE Select
|
NP_060814.4:p.Cys388Ser
|
|
NM_001174098.2:c.*392G>C
|
NP_001167569.1:n.*392G>C
|
|
NM_001363518.2:c.929G>C
|
NP_001350447.1:p.Cys310Ser
|
|
NR_033413.2:n.1131G>C
|
|
|
NR_033414.2:n.904G>C
|
|
|