ENST00000368485.8:c.1185G>T
MANE Select
|
ENSP00000357470.3:p.Arg395=
|
|
ENST00000344086.8:c.1091G>T
|
ENSP00000340589.4:p.Gly364Val
|
|
ENST00000368485.7:c.1185G>T
|
ENSP00000357470.3:p.Arg395=
|
|
ENST00000502679.1:n.498G>T
|
|
|
ENST00000507256.1:n.383G>T
|
|
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NM_000565.3:c.1185G>T
|
NP_000556.1:p.Arg395=
|
|
NM_181359.2:c.1091G>T
|
NP_852004.1:p.Gly364Val
|
|
XM_005245139.1:c.949G>T
|
XP_005245196.1:p.Gly317Cys
|
|
XM_005245140.1:c.*26G>T
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XP_005245197.1:n.*26G>T
|
|
XM_006711298.1:c.1233G>T
|
XP_006711361.1:p.Arg411=
|
|
XM_006711299.2:c.1139G>T
|
XP_006711362.1:p.Gly380Val
|
|
XM_005245139.2:c.949G>T
|
XP_005245196.1:p.Gly317Cys
|
|
XM_005245140.3:c.*26G>T
|
XP_005245197.1:n.*26G>T
|
|
XM_006711298.2:c.1233G>T
|
XP_006711361.1:p.Arg411=
|
|
XM_006711299.4:c.1139G>T
|
XP_006711362.1:p.Gly380Val
|
|
XM_017001199.2:c.1332G>T
|
XP_016856688.1:p.Arg444=
|
|
XM_017001200.2:c.1284G>T
|
XP_016856689.1:p.Arg428=
|
|
XM_017001201.2:c.*26G>T
|
XP_016856690.1:n.*26G>T
|
|
NM_000565.4:c.1185G>T
MANE Select
|
NP_000556.1:p.Arg395=
|
|
NM_181359.3:c.1091G>T
|
NP_852004.1:p.Gly364Val
|
|
NM_001382769.1:c.1284G>T
|
NP_001369698.1:p.Arg428=
|
|
NM_001382770.1:c.1278G>T
|
NP_001369699.1:p.Arg426=
|
|
NM_001382771.1:c.1233G>T
|
NP_001369700.1:p.Arg411=
|
|
NM_001382772.1:c.1179G>T
|
NP_001369701.1:p.Arg393=
|
|
NM_001382773.1:c.1139G>T
|
NP_001369702.1:p.Gly380Val
|
|
NM_001382774.1:c.825G>T
|
NP_001369703.1:p.Arg275=
|
|