ENST00000368485.8:c.961C>T
MANE Select
|
ENSP00000357470.3:p.Pro321Ser
|
|
ENST00000344086.8:c.961C>T
|
ENSP00000340589.4:p.Pro321Ser
|
|
ENST00000368485.7:c.961C>T
|
ENSP00000357470.3:p.Pro321Ser
|
|
ENST00000476006.5:c.777C>T
|
|
|
ENST00000507256.1:n.159C>T
|
|
|
ENST00000515190.1:c.369C>T
|
|
|
NM_000565.3:c.961C>T
|
NP_000556.1:p.Pro321Ser
|
|
NM_181359.2:c.961C>T
|
NP_852004.1:p.Pro321Ser
|
|
XM_005245139.1:c.819C>T
|
XP_005245196.1:p.Val273=
|
|
XM_005245140.1:c.819C>T
|
XP_005245197.1:p.Val273=
|
|
XM_006711298.1:c.1009C>T
|
XP_006711361.1:p.Pro337Ser
|
|
XM_006711299.2:c.1009C>T
|
XP_006711362.1:p.Pro337Ser
|
|
XM_005245139.2:c.819C>T
|
XP_005245196.1:p.Val273=
|
|
XM_005245140.3:c.819C>T
|
XP_005245197.1:p.Val273=
|
|
XM_006711298.2:c.1009C>T
|
XP_006711361.1:p.Pro337Ser
|
|
XM_006711299.4:c.1009C>T
|
XP_006711362.1:p.Pro337Ser
|
|
XM_017001199.2:c.1009C>T
|
XP_016856688.1:p.Pro337Ser
|
|
XM_017001200.2:c.961C>T
|
XP_016856689.1:p.Pro321Ser
|
|
XM_017001201.2:c.819C>T
|
XP_016856690.1:p.Val273=
|
|
NM_000565.4:c.961C>T
MANE Select
|
NP_000556.1:p.Pro321Ser
|
|
NM_181359.3:c.961C>T
|
NP_852004.1:p.Pro321Ser
|
|
NM_001382769.1:c.961C>T
|
NP_001369698.1:p.Pro321Ser
|
|
NM_001382770.1:c.1054C>T
|
NP_001369699.1:p.Pro352Ser
|
|
NM_001382771.1:c.1009C>T
|
NP_001369700.1:p.Pro337Ser
|
|
NM_001382772.1:c.955C>T
|
NP_001369701.1:p.Pro319Ser
|
|
NM_001382773.1:c.1009C>T
|
NP_001369702.1:p.Pro337Ser
|
|
NM_001382774.1:c.601C>T
|
NP_001369703.1:p.Pro201Ser
|
|