ENST00000368485.8:c.1192A>T
MANE Select
|
ENSP00000357470.3:p.Lys398Ter
|
|
ENST00000344086.8:c.1098A>T
|
ENSP00000340589.4:p.Ter366Cys
|
|
ENST00000368485.7:c.1192A>T
|
ENSP00000357470.3:p.Lys398Ter
|
|
ENST00000502679.1:n.505A>T
|
|
|
ENST00000507256.1:n.390A>T
|
|
|
NM_000565.3:c.1192A>T
|
NP_000556.1:p.Lys398Ter
|
|
NM_181359.2:c.1098A>T
|
NP_852004.1:p.Ter366Cys
|
|
XM_005245139.1:c.956A>T
|
XP_005245196.1:p.Glu319Val
|
|
XM_005245140.1:c.*33A>T
|
XP_005245197.1:n.*33A>T
|
|
XM_006711298.1:c.1240A>T
|
XP_006711361.1:p.Lys414Ter
|
|
XM_006711299.2:c.1146A>T
|
XP_006711362.1:p.Ter382Cys
|
|
XM_005245139.2:c.956A>T
|
XP_005245196.1:p.Glu319Val
|
|
XM_005245140.3:c.*33A>T
|
XP_005245197.1:n.*33A>T
|
|
XM_006711298.2:c.1240A>T
|
XP_006711361.1:p.Lys414Ter
|
|
XM_006711299.4:c.1146A>T
|
XP_006711362.1:p.Ter382Cys
|
|
XM_017001199.2:c.1339A>T
|
XP_016856688.1:p.Lys447Ter
|
|
XM_017001200.2:c.1291A>T
|
XP_016856689.1:p.Lys431Ter
|
|
XM_017001201.2:c.*33A>T
|
XP_016856690.1:n.*33A>T
|
|
NM_000565.4:c.1192A>T
MANE Select
|
NP_000556.1:p.Lys398Ter
|
|
NM_181359.3:c.1098A>T
|
NP_852004.1:p.Ter366Cys
|
|
NM_001382769.1:c.1291A>T
|
NP_001369698.1:p.Lys431Ter
|
|
NM_001382770.1:c.1285A>T
|
NP_001369699.1:p.Lys429Ter
|
|
NM_001382771.1:c.1240A>T
|
NP_001369700.1:p.Lys414Ter
|
|
NM_001382772.1:c.1186A>T
|
NP_001369701.1:p.Lys396Ter
|
|
NM_001382773.1:c.1146A>T
|
NP_001369702.1:p.Ter382Cys
|
|
NM_001382774.1:c.832A>T
|
NP_001369703.1:p.Lys278Ter
|
|