ENST00000352909.8:c.833T>C
MANE Select
|
ENSP00000325951.4:p.Phe278Ser
|
|
ENST00000324155.8:c.*522T>C
|
ENSP00000325831.3:n.*522T>C
|
|
ENST00000333684.9:c.696-346T>C
|
ENSP00000328814.6:n.696-346T>C
|
|
ENST00000352909.7:c.833T>C
|
ENSP00000325951.3:p.Phe278Ser
|
|
ENST00000381168.7:c.*553T>C
|
ENSP00000370560.3:n.*553T>C
|
|
ENST00000381175.5:c.914T>C
|
ENSP00000370567.1:p.Phe305Ser
|
|
ENST00000381178.5:c.926T>C
|
ENSP00000370571.1:p.Phe309Ser
|
|
ENST00000412076.1:c.136-346T>C
|
|
|
ENST00000416223.5:c.136-127T>C
|
|
|
ENST00000469226.1:n.962T>C
|
|
|
ENST00000479437.5:n.382T>C
|
|
|
NM_000360.3:c.833T>C
|
NP_000351.2:p.Phe278Ser
|
|
NM_199292.2:c.926T>C
|
NP_954986.2:p.Phe309Ser
|
|
NM_199293.2:c.914T>C
|
NP_954987.2:p.Phe305Ser
|
|
XM_011520335.1:c.845T>C
|
XP_011518637.1:p.Phe282Ser
|
|
XM_011520335.2:c.845T>C
|
XP_011518637.1:p.Phe282Ser
|
|
NM_000360.4:c.833T>C
MANE Select
|
NP_000351.2:p.Phe278Ser
|
|
NM_199292.3:c.926T>C
|
NP_954986.2:p.Phe309Ser
|
|
NM_199293.3:c.914T>C
|
NP_954987.2:p.Phe305Ser
|
|