ENST00000368485.8:c.1069C>T
MANE Select
|
ENSP00000357470.3:p.Gln357Ter
|
|
ENST00000344086.8:c.1066+4510C>T
|
ENSP00000340589.4:n.1066+4510C>T
|
|
ENST00000368485.7:c.1069C>T
|
ENSP00000357470.3:p.Gln357Ter
|
|
ENST00000502679.1:n.382C>T
|
|
|
ENST00000507256.1:n.267C>T
|
|
|
ENST00000515190.1:c.477C>T
|
|
|
NM_000565.3:c.1069C>T
|
NP_000556.1:p.Gln357Ter
|
|
NM_181359.2:c.1066+4510C>T
|
NP_852004.1:n.1066+4510C>T
|
|
XM_005245139.1:c.924+4510C>T
|
XP_005245196.1:n.924+4510C>T
|
|
XM_005245140.1:c.927C>T
|
XP_005245197.1:p.Cys309=
|
|
XM_006711298.1:c.1117C>T
|
XP_006711361.1:p.Gln373Ter
|
|
XM_006711299.2:c.1114+4510C>T
|
XP_006711362.1:n.1114+4510C>T
|
|
XM_005245139.2:c.924+4510C>T
|
XP_005245196.1:n.924+4510C>T
|
|
XM_005245140.3:c.927C>T
|
XP_005245197.1:p.Cys309=
|
|
XM_006711298.2:c.1117C>T
|
XP_006711361.1:p.Gln373Ter
|
|
XM_006711299.4:c.1114+4510C>T
|
XP_006711362.1:n.1114+4510C>T
|
|
XM_017001199.2:c.1216C>T
|
XP_016856688.1:p.Gln406Ter
|
|
XM_017001200.2:c.1168C>T
|
XP_016856689.1:p.Gln390Ter
|
|
XM_017001201.2:c.1026C>T
|
XP_016856690.1:p.Cys342=
|
|
NM_000565.4:c.1069C>T
MANE Select
|
NP_000556.1:p.Gln357Ter
|
|
NM_181359.3:c.1066+4510C>T
|
NP_852004.1:n.1066+4510C>T
|
|
NM_001382769.1:c.1168C>T
|
NP_001369698.1:p.Gln390Ter
|
|
NM_001382770.1:c.1162C>T
|
NP_001369699.1:p.Gln388Ter
|
|
NM_001382771.1:c.1117C>T
|
NP_001369700.1:p.Gln373Ter
|
|
NM_001382772.1:c.1063C>T
|
NP_001369701.1:p.Gln355Ter
|
|
NM_001382773.1:c.1114+4510C>T
|
NP_001369702.1:n.1114+4510C>T
|
|
NM_001382774.1:c.709C>T
|
NP_001369703.1:p.Gln237Ter
|
|