ENST00000368485.8:c.1234C>T
MANE Select
|
ENSP00000357470.3:p.Gln412Ter
|
|
ENST00000344086.8:c.*42C>T
|
ENSP00000340589.4:n.*42C>T
|
|
ENST00000368485.7:c.1234C>T
|
ENSP00000357470.3:p.Gln412Ter
|
|
ENST00000502679.1:n.547C>T
|
|
|
ENST00000507256.1:n.432C>T
|
|
|
NM_000565.3:c.1234C>T
|
NP_000556.1:p.Gln412Ter
|
|
NM_181359.2:c.*42C>T
|
NP_852004.1:n.*42C>T
|
|
XM_005245139.1:c.998C>T
|
XP_005245196.1:p.Ala333Val
|
|
XM_005245140.1:c.*75C>T
|
XP_005245197.1:n.*75C>T
|
|
XM_006711298.1:c.1282C>T
|
XP_006711361.1:p.Gln428Ter
|
|
XM_006711299.2:c.*42C>T
|
XP_006711362.1:n.*42C>T
|
|
XM_005245139.2:c.998C>T
|
XP_005245196.1:p.Ala333Val
|
|
XM_005245140.3:c.*75C>T
|
XP_005245197.1:n.*75C>T
|
|
XM_006711298.2:c.1282C>T
|
XP_006711361.1:p.Gln428Ter
|
|
XM_006711299.4:c.*42C>T
|
XP_006711362.1:n.*42C>T
|
|
XM_017001199.2:c.1381C>T
|
XP_016856688.1:p.Gln461Ter
|
|
XM_017001200.2:c.1333C>T
|
XP_016856689.1:p.Gln445Ter
|
|
XM_017001201.2:c.*75C>T
|
XP_016856690.1:n.*75C>T
|
|
NM_000565.4:c.1234C>T
MANE Select
|
NP_000556.1:p.Gln412Ter
|
|
NM_181359.3:c.*42C>T
|
NP_852004.1:n.*42C>T
|
|
NM_001382769.1:c.1333C>T
|
NP_001369698.1:p.Gln445Ter
|
|
NM_001382770.1:c.1327C>T
|
NP_001369699.1:p.Gln443Ter
|
|
NM_001382771.1:c.1282C>T
|
NP_001369700.1:p.Gln428Ter
|
|
NM_001382772.1:c.1228C>T
|
NP_001369701.1:p.Gln410Ter
|
|
NM_001382773.1:c.*42C>T
|
NP_001369702.1:n.*42C>T
|
|
NM_001382774.1:c.874C>T
|
NP_001369703.1:p.Gln292Ter
|
|