ENST00000697843.1:n.2602A>G
|
|
|
ENST00000373189.6:c.1126A>G
MANE Select
|
ENSP00000362285.5:p.Ser376Gly
|
|
ENST00000479577.2:c.892A>G
|
ENSP00000493995.1:p.Ser298Gly
|
|
ENST00000642198.1:c.*698A>G
|
ENSP00000494827.1:n.*698A>G
|
|
ENST00000642772.1:c.*94+6063A>G
|
ENSP00000495041.1:n.*94+6063A>G
|
|
ENST00000643042.1:c.747A>G
|
ENSP00000496674.1:n.747A>G
|
|
ENST00000643619.1:c.*709A>G
|
ENSP00000494378.1:n.*709A>G
|
|
ENST00000643752.1:c.*452A>G
|
ENSP00000495000.1:n.*452A>G
|
|
ENST00000644088.1:c.*447A>G
|
ENSP00000494066.1:n.*447A>G
|
|
ENST00000644591.1:c.*452A>G
|
ENSP00000496664.1:n.*452A>G
|
|
ENST00000644895.1:c.*99+6063A>G
|
ENSP00000493872.1:n.*99+6063A>G
|
|
ENST00000645345.1:c.*698A>G
|
ENSP00000495859.1:n.*698A>G
|
|
ENST00000647524.1:c.*709A>G
|
ENSP00000495077.1:n.*709A>G
|
|
ENST00000373189.5:c.1126A>G
|
ENSP00000362285.5:p.Ser376Gly
|
|
ENST00000469204.1:n.623A>G
|
|
|
NM_001174098.1:c.*355A>G
|
NP_001167569.1:n.*355A>G
|
|
NM_018344.5:c.1126A>G
|
NP_060814.4:p.Ser376Gly
|
|
NR_033413.1:n.1100A>G
|
|
|
NR_033414.1:n.873A>G
|
|
|
XM_006717910.2:c.892A>G
|
XP_006717973.1:p.Ser298Gly
|
|
NM_001363518.1:c.892A>G
|
NP_001350447.1:p.Ser298Gly
|
|
XM_017016377.2:c.688A>G
|
XP_016871866.1:p.Ser230Gly
|
|
XM_017016378.2:c.508A>G
|
XP_016871867.1:p.Ser170Gly
|
|
NM_018344.6:c.1126A>G
MANE Select
|
NP_060814.4:p.Ser376Gly
|
|
NM_001174098.2:c.*355A>G
|
NP_001167569.1:n.*355A>G
|
|
NM_001363518.2:c.892A>G
|
NP_001350447.1:p.Ser298Gly
|
|
NR_033413.2:n.1094A>G
|
|
|
NR_033414.2:n.867A>G
|
|
|