ENST00000402673.7:c.527T>C
MANE Select
|
ENSP00000385432.2:p.Phe176Ser
|
|
ENST00000402673.6:c.527T>C
|
ENSP00000385432.2:p.Phe176Ser
|
|
ENST00000439578.5:c.527T>C
|
ENSP00000404997.1:p.Phe176Ser
|
|
ENST00000502539.5:c.323T>C
|
ENSP00000426335.1:p.Phe108Ser
|
|
ENST00000503318.5:c.*250T>C
|
ENSP00000425367.1:n.*250T>C
|
|
ENST00000507419.5:c.323T>C
|
ENSP00000425339.1:p.Phe108Ser
|
|
ENST00000508363.5:n.2496T>C
|
|
|
ENST00000509730.5:c.323T>C
|
ENSP00000423197.1:p.Phe108Ser
|
|
ENST00000509937.5:c.323T>C
|
ENSP00000424673.1:p.Phe108Ser
|
|
NM_001033503.2:c.527T>C
|
NP_001028675.1:p.Phe176Ser
|
|
NM_016103.3:c.527T>C
|
NP_057187.1:p.Phe176Ser
|
|
NM_016103.4:c.527T>C
MANE Select
|
NP_057187.1:p.Phe176Ser
|
|
NM_001033503.3:c.527T>C
|
NP_001028675.1:p.Phe176Ser
|
|