ENST00000368485.8:c.1163T>C
MANE Select
|
ENSP00000357470.3:p.Phe388Ser
|
|
ENST00000344086.8:c.1069T>C
|
ENSP00000340589.4:p.Ser357Pro
|
|
ENST00000368485.7:c.1163T>C
|
ENSP00000357470.3:p.Phe388Ser
|
|
ENST00000502679.1:n.476T>C
|
|
|
ENST00000507256.1:n.361T>C
|
|
|
NM_000565.3:c.1163T>C
|
NP_000556.1:p.Phe388Ser
|
|
NM_181359.2:c.1069T>C
|
NP_852004.1:p.Ser357Pro
|
|
XM_005245139.1:c.927T>C
|
XP_005245196.1:p.Val309=
|
|
XM_005245140.1:c.*4T>C
|
XP_005245197.1:n.*4T>C
|
|
XM_006711298.1:c.1211T>C
|
XP_006711361.1:p.Phe404Ser
|
|
XM_006711299.2:c.1117T>C
|
XP_006711362.1:p.Ser373Pro
|
|
XM_005245139.2:c.927T>C
|
XP_005245196.1:p.Val309=
|
|
XM_005245140.3:c.*4T>C
|
XP_005245197.1:n.*4T>C
|
|
XM_006711298.2:c.1211T>C
|
XP_006711361.1:p.Phe404Ser
|
|
XM_006711299.4:c.1117T>C
|
XP_006711362.1:p.Ser373Pro
|
|
XM_017001199.2:c.1310T>C
|
XP_016856688.1:p.Phe437Ser
|
|
XM_017001200.2:c.1262T>C
|
XP_016856689.1:p.Phe421Ser
|
|
XM_017001201.2:c.*4T>C
|
XP_016856690.1:n.*4T>C
|
|
NM_000565.4:c.1163T>C
MANE Select
|
NP_000556.1:p.Phe388Ser
|
|
NM_181359.3:c.1069T>C
|
NP_852004.1:p.Ser357Pro
|
|
NM_001382769.1:c.1262T>C
|
NP_001369698.1:p.Phe421Ser
|
|
NM_001382770.1:c.1256T>C
|
NP_001369699.1:p.Phe419Ser
|
|
NM_001382771.1:c.1211T>C
|
NP_001369700.1:p.Phe404Ser
|
|
NM_001382772.1:c.1157T>C
|
NP_001369701.1:p.Phe386Ser
|
|
NM_001382773.1:c.1117T>C
|
NP_001369702.1:p.Ser373Pro
|
|
NM_001382774.1:c.803T>C
|
NP_001369703.1:p.Phe268Ser
|
|