ENST00000368485.8:c.1251G>C
MANE Select
|
ENSP00000357470.3:p.Arg417Ser
|
|
ENST00000344086.8:c.*59G>C
|
ENSP00000340589.4:n.*59G>C
|
|
ENST00000368485.7:c.1251G>C
|
ENSP00000357470.3:p.Arg417Ser
|
|
ENST00000502679.1:n.564G>C
|
|
|
ENST00000507256.1:n.449G>C
|
|
|
NM_000565.3:c.1251G>C
|
NP_000556.1:p.Arg417Ser
|
|
NM_181359.2:c.*59G>C
|
NP_852004.1:n.*59G>C
|
|
XM_005245139.1:c.1015G>C
|
XP_005245196.1:p.Ala339Pro
|
|
XM_005245140.1:c.*92G>C
|
XP_005245197.1:n.*92G>C
|
|
XM_006711298.1:c.1299G>C
|
XP_006711361.1:p.Arg433Ser
|
|
XM_006711299.2:c.*59G>C
|
XP_006711362.1:n.*59G>C
|
|
XM_005245139.2:c.1015G>C
|
XP_005245196.1:p.Ala339Pro
|
|
XM_005245140.3:c.*92G>C
|
XP_005245197.1:n.*92G>C
|
|
XM_006711298.2:c.1299G>C
|
XP_006711361.1:p.Arg433Ser
|
|
XM_006711299.4:c.*59G>C
|
XP_006711362.1:n.*59G>C
|
|
XM_017001199.2:c.1398G>C
|
XP_016856688.1:p.Arg466Ser
|
|
XM_017001200.2:c.1350G>C
|
XP_016856689.1:p.Arg450Ser
|
|
XM_017001201.2:c.*92G>C
|
XP_016856690.1:n.*92G>C
|
|
NM_000565.4:c.1251G>C
MANE Select
|
NP_000556.1:p.Arg417Ser
|
|
NM_181359.3:c.*59G>C
|
NP_852004.1:n.*59G>C
|
|
NM_001382769.1:c.1350G>C
|
NP_001369698.1:p.Arg450Ser
|
|
NM_001382770.1:c.1344G>C
|
NP_001369699.1:p.Arg448Ser
|
|
NM_001382771.1:c.1299G>C
|
NP_001369700.1:p.Arg433Ser
|
|
NM_001382772.1:c.1245G>C
|
NP_001369701.1:p.Arg415Ser
|
|
NM_001382773.1:c.*59G>C
|
NP_001369702.1:n.*59G>C
|
|
NM_001382774.1:c.891G>C
|
NP_001369703.1:p.Arg297Ser
|
|