ENST00000352909.8:c.905G=
MANE Select
|
ENSP00000325951.4:p.Ser302=
|
|
ENST00000324155.8:c.*594G=
|
ENSP00000325831.3:n.*594G=
|
|
ENST00000333684.9:c.696-156G=
|
ENSP00000328814.6:n.696-156G=
|
|
ENST00000352909.7:c.905G=
|
ENSP00000325951.3:p.Ser302=
|
|
ENST00000381168.7:c.*625G=
|
ENSP00000370560.3:n.*625G=
|
|
ENST00000381175.5:c.986G=
|
ENSP00000370567.1:p.Ser329=
|
|
ENST00000381178.5:c.998G=
|
ENSP00000370571.1:p.Ser333=
|
|
ENST00000412076.1:c.136-156G=
|
|
|
ENST00000416223.5:c.199G=
|
|
|
ENST00000461172.1:n.70G=
|
|
|
ENST00000479437.5:n.454G=
|
|
|
NM_000360.3:c.905G=
|
NP_000351.2:p.Ser302=
|
|
NM_199292.2:c.998G=
|
NP_954986.2:p.Ser333=
|
|
NM_199293.2:c.986G=
|
NP_954987.2:p.Ser329=
|
|
XM_011520335.1:c.917G=
|
XP_011518637.1:p.Ser306=
|
|
XM_011520335.2:c.917G=
|
XP_011518637.1:p.Ser306=
|
|
NM_000360.4:c.905G=
MANE Select
|
NP_000351.2:p.Ser302=
|
|
NM_199292.3:c.998G=
|
NP_954986.2:p.Ser333=
|
|
NM_199293.3:c.986G=
|
NP_954987.2:p.Ser329=
|
|