ENST00000368485.8:c.1298C>T
MANE Select
|
ENSP00000357470.3:p.Ser433Phe
|
|
ENST00000344086.8:c.*106C>T
|
ENSP00000340589.4:n.*106C>T
|
|
ENST00000368485.7:c.1298C>T
|
ENSP00000357470.3:p.Ser433Phe
|
|
ENST00000507256.1:n.496C>T
|
|
|
NM_000565.3:c.1298C>T
|
NP_000556.1:p.Ser433Phe
|
|
NM_181359.2:c.*106C>T
|
NP_852004.1:n.*106C>T
|
|
XM_005245139.1:c.1062C>T
|
XP_005245196.1:p.Val354=
|
|
XM_005245140.1:c.*139C>T
|
XP_005245197.1:n.*139C>T
|
|
XM_006711298.1:c.1346C>T
|
XP_006711361.1:p.Ser449Phe
|
|
XM_005245139.2:c.1062C>T
|
XP_005245196.1:p.Val354=
|
|
XM_005245140.3:c.*139C>T
|
XP_005245197.1:n.*139C>T
|
|
XM_006711298.2:c.1346C>T
|
XP_006711361.1:p.Ser449Phe
|
|
XM_017001199.2:c.1445C>T
|
XP_016856688.1:p.Ser482Phe
|
|
XM_017001200.2:c.1397C>T
|
XP_016856689.1:p.Ser466Phe
|
|
XM_017001201.2:c.*139C>T
|
XP_016856690.1:n.*139C>T
|
|
NM_000565.4:c.1298C>T
MANE Select
|
NP_000556.1:p.Ser433Phe
|
|
NM_181359.3:c.*106C>T
|
NP_852004.1:n.*106C>T
|
|
NM_001382769.1:c.1397C>T
|
NP_001369698.1:p.Ser466Phe
|
|
NM_001382770.1:c.1391C>T
|
NP_001369699.1:p.Ser464Phe
|
|
NM_001382771.1:c.1346C>T
|
NP_001369700.1:p.Ser449Phe
|
|
NM_001382772.1:c.1292C>T
|
NP_001369701.1:p.Ser431Phe
|
|
NM_001382773.1:c.*106C>T
|
NP_001369702.1:n.*106C>T
|
|
NM_001382774.1:c.938C>T
|
NP_001369703.1:p.Ser313Phe
|
|