ENST00000352909.8:c.696G>A
MANE Select
|
ENSP00000325951.4:p.Trp232Ter
|
|
ENST00000324155.8:c.*385G>A
|
ENSP00000325831.3:n.*385G>A
|
|
ENST00000333684.9:c.695+403G>A
|
ENSP00000328814.6:n.695+403G>A
|
|
ENST00000352909.7:c.696G>A
|
ENSP00000325951.3:p.Trp232Ter
|
|
ENST00000381168.7:c.*416G>A
|
ENSP00000370560.3:n.*416G>A
|
|
ENST00000381175.5:c.777G>A
|
ENSP00000370567.1:p.Trp259Ter
|
|
ENST00000381178.5:c.789G>A
|
ENSP00000370571.1:p.Trp263Ter
|
|
ENST00000412076.1:c.135+403G>A
|
|
|
ENST00000416223.5:c.136-264G>A
|
|
|
ENST00000469226.1:n.825G>A
|
|
|
ENST00000479437.5:n.245G>A
|
|
|
NM_000360.3:c.696G>A
|
NP_000351.2:p.Trp232Ter
|
|
NM_199292.2:c.789G>A
|
NP_954986.2:p.Trp263Ter
|
|
NM_199293.2:c.777G>A
|
NP_954987.2:p.Trp259Ter
|
|
XM_011520335.1:c.708G>A
|
XP_011518637.1:p.Trp236Ter
|
|
XM_011520335.2:c.708G>A
|
XP_011518637.1:p.Trp236Ter
|
|
NM_000360.4:c.696G>A
MANE Select
|
NP_000351.2:p.Trp232Ter
|
|
NM_199292.3:c.789G>A
|
NP_954986.2:p.Trp263Ter
|
|
NM_199293.3:c.777G>A
|
NP_954987.2:p.Trp259Ter
|
|