ENST00000368485.8:c.1306A>C
MANE Select
|
ENSP00000357470.3:p.Ser436Arg
|
|
ENST00000344086.8:c.*114A>C
|
ENSP00000340589.4:n.*114A>C
|
|
ENST00000368485.7:c.1306A>C
|
ENSP00000357470.3:p.Ser436Arg
|
|
ENST00000507256.1:n.504A>C
|
|
|
NM_000565.3:c.1306A>C
|
NP_000556.1:p.Ser436Arg
|
|
NM_181359.2:c.*114A>C
|
NP_852004.1:n.*114A>C
|
|
XM_005245139.1:c.1070A>C
|
XP_005245196.1:p.Gln357Pro
|
|
XM_005245140.1:c.*147A>C
|
XP_005245197.1:n.*147A>C
|
|
XM_006711298.1:c.1354A>C
|
XP_006711361.1:p.Ser452Arg
|
|
XM_005245139.2:c.1070A>C
|
XP_005245196.1:p.Gln357Pro
|
|
XM_005245140.3:c.*147A>C
|
XP_005245197.1:n.*147A>C
|
|
XM_006711298.2:c.1354A>C
|
XP_006711361.1:p.Ser452Arg
|
|
XM_017001199.2:c.1453A>C
|
XP_016856688.1:p.Ser485Arg
|
|
XM_017001200.2:c.1405A>C
|
XP_016856689.1:p.Ser469Arg
|
|
XM_017001201.2:c.*147A>C
|
XP_016856690.1:n.*147A>C
|
|
NM_000565.4:c.1306A>C
MANE Select
|
NP_000556.1:p.Ser436Arg
|
|
NM_181359.3:c.*114A>C
|
NP_852004.1:n.*114A>C
|
|
NM_001382769.1:c.1405A>C
|
NP_001369698.1:p.Ser469Arg
|
|
NM_001382770.1:c.1399A>C
|
NP_001369699.1:p.Ser467Arg
|
|
NM_001382771.1:c.1354A>C
|
NP_001369700.1:p.Ser452Arg
|
|
NM_001382772.1:c.1300A>C
|
NP_001369701.1:p.Ser434Arg
|
|
NM_001382773.1:c.*114A>C
|
NP_001369702.1:n.*114A>C
|
|
NM_001382774.1:c.946A>C
|
NP_001369703.1:p.Ser316Arg
|
|