ENST00000352909.8:c.932C>T
MANE Select
|
ENSP00000325951.4:p.Thr311Ile
|
|
ENST00000324155.8:c.*621C>T
|
ENSP00000325831.3:n.*621C>T
|
|
ENST00000333684.9:c.696-129C>T
|
ENSP00000328814.6:n.696-129C>T
|
|
ENST00000352909.7:c.932C>T
|
ENSP00000325951.3:p.Thr311Ile
|
|
ENST00000381168.7:c.*652C>T
|
ENSP00000370560.3:n.*652C>T
|
|
ENST00000381175.5:c.1013C>T
|
ENSP00000370567.1:p.Thr338Ile
|
|
ENST00000381178.5:c.1025C>T
|
ENSP00000370571.1:p.Thr342Ile
|
|
ENST00000412076.1:c.136-129C>T
|
|
|
ENST00000416223.5:c.226C>T
|
|
|
ENST00000461172.1:n.97C>T
|
|
|
ENST00000479437.5:n.481C>T
|
|
|
NM_000360.3:c.932C>T
|
NP_000351.2:p.Thr311Ile
|
|
NM_199292.2:c.1025C>T
|
NP_954986.2:p.Thr342Ile
|
|
NM_199293.2:c.1013C>T
|
NP_954987.2:p.Thr338Ile
|
|
XM_011520335.1:c.944C>T
|
XP_011518637.1:p.Thr315Ile
|
|
XM_011520335.2:c.944C>T
|
XP_011518637.1:p.Thr315Ile
|
|
NM_000360.4:c.932C>T
MANE Select
|
NP_000351.2:p.Thr311Ile
|
|
NM_199292.3:c.1025C>T
|
NP_954986.2:p.Thr342Ile
|
|
NM_199293.3:c.1013C>T
|
NP_954987.2:p.Thr338Ile
|
|