ENST00000368485.8:c.1206A>G
MANE Select
|
ENSP00000357470.3:p.Thr402=
|
|
ENST00000344086.8:c.*14A>G
|
ENSP00000340589.4:n.*14A>G
|
|
ENST00000368485.7:c.1206A>G
|
ENSP00000357470.3:p.Thr402=
|
|
ENST00000502679.1:n.519A>G
|
|
|
ENST00000507256.1:n.404A>G
|
|
|
NM_000565.3:c.1206A>G
|
NP_000556.1:p.Thr402=
|
|
NM_181359.2:c.*14A>G
|
NP_852004.1:n.*14A>G
|
|
XM_005245139.1:c.970A>G
|
XP_005245196.1:p.Lys324Glu
|
|
XM_005245140.1:c.*47A>G
|
XP_005245197.1:n.*47A>G
|
|
XM_006711298.1:c.1254A>G
|
XP_006711361.1:p.Thr418=
|
|
XM_006711299.2:c.*14A>G
|
XP_006711362.1:n.*14A>G
|
|
XM_005245139.2:c.970A>G
|
XP_005245196.1:p.Lys324Glu
|
|
XM_005245140.3:c.*47A>G
|
XP_005245197.1:n.*47A>G
|
|
XM_006711298.2:c.1254A>G
|
XP_006711361.1:p.Thr418=
|
|
XM_006711299.4:c.*14A>G
|
XP_006711362.1:n.*14A>G
|
|
XM_017001199.2:c.1353A>G
|
XP_016856688.1:p.Thr451=
|
|
XM_017001200.2:c.1305A>G
|
XP_016856689.1:p.Thr435=
|
|
XM_017001201.2:c.*47A>G
|
XP_016856690.1:n.*47A>G
|
|
NM_000565.4:c.1206A>G
MANE Select
|
NP_000556.1:p.Thr402=
|
|
NM_181359.3:c.*14A>G
|
NP_852004.1:n.*14A>G
|
|
NM_001382769.1:c.1305A>G
|
NP_001369698.1:p.Thr435=
|
|
NM_001382770.1:c.1299A>G
|
NP_001369699.1:p.Thr433=
|
|
NM_001382771.1:c.1254A>G
|
NP_001369700.1:p.Thr418=
|
|
NM_001382772.1:c.1200A>G
|
NP_001369701.1:p.Thr400=
|
|
NM_001382773.1:c.*14A>G
|
NP_001369702.1:n.*14A>G
|
|
NM_001382774.1:c.846A>G
|
NP_001369703.1:p.Thr282=
|
|