ENST00000368485.8:c.1219C>T
MANE Select
|
ENSP00000357470.3:p.Pro407Ser
|
|
ENST00000344086.8:c.*27C>T
|
ENSP00000340589.4:n.*27C>T
|
|
ENST00000368485.7:c.1219C>T
|
ENSP00000357470.3:p.Pro407Ser
|
|
ENST00000502679.1:n.532C>T
|
|
|
ENST00000507256.1:n.417C>T
|
|
|
NM_000565.3:c.1219C>T
|
NP_000556.1:p.Pro407Ser
|
|
NM_181359.2:c.*27C>T
|
NP_852004.1:n.*27C>T
|
|
XM_005245139.1:c.983C>T
|
XP_005245196.1:p.Ala328Val
|
|
XM_005245140.1:c.*60C>T
|
XP_005245197.1:n.*60C>T
|
|
XM_006711298.1:c.1267C>T
|
XP_006711361.1:p.Pro423Ser
|
|
XM_006711299.2:c.*27C>T
|
XP_006711362.1:n.*27C>T
|
|
XM_005245139.2:c.983C>T
|
XP_005245196.1:p.Ala328Val
|
|
XM_005245140.3:c.*60C>T
|
XP_005245197.1:n.*60C>T
|
|
XM_006711298.2:c.1267C>T
|
XP_006711361.1:p.Pro423Ser
|
|
XM_006711299.4:c.*27C>T
|
XP_006711362.1:n.*27C>T
|
|
XM_017001199.2:c.1366C>T
|
XP_016856688.1:p.Pro456Ser
|
|
XM_017001200.2:c.1318C>T
|
XP_016856689.1:p.Pro440Ser
|
|
XM_017001201.2:c.*60C>T
|
XP_016856690.1:n.*60C>T
|
|
NM_000565.4:c.1219C>T
MANE Select
|
NP_000556.1:p.Pro407Ser
|
|
NM_181359.3:c.*27C>T
|
NP_852004.1:n.*27C>T
|
|
NM_001382769.1:c.1318C>T
|
NP_001369698.1:p.Pro440Ser
|
|
NM_001382770.1:c.1312C>T
|
NP_001369699.1:p.Pro438Ser
|
|
NM_001382771.1:c.1267C>T
|
NP_001369700.1:p.Pro423Ser
|
|
NM_001382772.1:c.1213C>T
|
NP_001369701.1:p.Pro405Ser
|
|
NM_001382773.1:c.*27C>T
|
NP_001369702.1:n.*27C>T
|
|
NM_001382774.1:c.859C>T
|
NP_001369703.1:p.Pro287Ser
|
|