ENST00000352909.8:c.1031T>C
MANE Select
|
ENSP00000325951.4:p.Phe344Ser
|
|
ENST00000324155.8:c.*720T>C
|
ENSP00000325831.3:n.*720T>C
|
|
ENST00000333684.9:c.749T>C
|
ENSP00000328814.6:p.Phe250Ser
|
|
ENST00000352909.7:c.1031T>C
|
ENSP00000325951.3:p.Phe344Ser
|
|
ENST00000381168.7:c.*751T>C
|
ENSP00000370560.3:n.*751T>C
|
|
ENST00000381175.5:c.1112T>C
|
ENSP00000370567.1:p.Phe371Ser
|
|
ENST00000381178.5:c.1124T>C
|
ENSP00000370571.1:p.Phe375Ser
|
|
ENST00000412076.1:c.189T>C
|
|
|
ENST00000416223.5:c.325T>C
|
|
|
ENST00000461172.1:n.196T>C
|
|
|
ENST00000479437.5:n.580T>C
|
|
|
NM_000360.3:c.1031T>C
|
NP_000351.2:p.Phe344Ser
|
|
NM_199292.2:c.1124T>C
|
NP_954986.2:p.Phe375Ser
|
|
NM_199293.2:c.1112T>C
|
NP_954987.2:p.Phe371Ser
|
|
XM_011520335.1:c.1043T>C
|
XP_011518637.1:p.Phe348Ser
|
|
XM_011520335.2:c.1043T>C
|
XP_011518637.1:p.Phe348Ser
|
|
NM_000360.4:c.1031T>C
MANE Select
|
NP_000351.2:p.Phe344Ser
|
|
NM_199292.3:c.1124T>C
|
NP_954986.2:p.Phe375Ser
|
|
NM_199293.3:c.1112T>C
|
NP_954987.2:p.Phe371Ser
|
|