ENST00000368485.8:c.986C>G
MANE Select
|
ENSP00000357470.3:p.Thr329Ser
|
|
ENST00000344086.8:c.986C>G
|
ENSP00000340589.4:p.Thr329Ser
|
|
ENST00000368485.7:c.986C>G
|
ENSP00000357470.3:p.Thr329Ser
|
|
ENST00000476006.5:c.802C>G
|
|
|
ENST00000507256.1:n.184C>G
|
|
|
ENST00000515190.1:c.394C>G
|
|
|
NM_000565.3:c.986C>G
|
NP_000556.1:p.Thr329Ser
|
|
NM_181359.2:c.986C>G
|
NP_852004.1:p.Thr329Ser
|
|
XM_005245139.1:c.844C>G
|
XP_005245196.1:p.Pro282Ala
|
|
XM_005245140.1:c.844C>G
|
XP_005245197.1:p.Pro282Ala
|
|
XM_006711298.1:c.1034C>G
|
XP_006711361.1:p.Thr345Ser
|
|
XM_006711299.2:c.1034C>G
|
XP_006711362.1:p.Thr345Ser
|
|
XM_005245139.2:c.844C>G
|
XP_005245196.1:p.Pro282Ala
|
|
XM_005245140.3:c.844C>G
|
XP_005245197.1:p.Pro282Ala
|
|
XM_006711298.2:c.1034C>G
|
XP_006711361.1:p.Thr345Ser
|
|
XM_006711299.4:c.1034C>G
|
XP_006711362.1:p.Thr345Ser
|
|
XM_017001199.2:c.1034C>G
|
XP_016856688.1:p.Thr345Ser
|
|
XM_017001200.2:c.986C>G
|
XP_016856689.1:p.Thr329Ser
|
|
XM_017001201.2:c.844C>G
|
XP_016856690.1:p.Pro282Ala
|
|
NM_000565.4:c.986C>G
MANE Select
|
NP_000556.1:p.Thr329Ser
|
|
NM_181359.3:c.986C>G
|
NP_852004.1:p.Thr329Ser
|
|
NM_001382769.1:c.986C>G
|
NP_001369698.1:p.Thr329Ser
|
|
NM_001382770.1:c.1079C>G
|
NP_001369699.1:p.Thr360Ser
|
|
NM_001382771.1:c.1034C>G
|
NP_001369700.1:p.Thr345Ser
|
|
NM_001382772.1:c.980C>G
|
NP_001369701.1:p.Thr327Ser
|
|
NM_001382773.1:c.1034C>G
|
NP_001369702.1:p.Thr345Ser
|
|
NM_001382774.1:c.626C>G
|
NP_001369703.1:p.Thr209Ser
|
|