ENST00000352909.8:c.875G=
MANE Select
|
ENSP00000325951.4:p.Gly292=
|
|
ENST00000324155.8:c.*564G=
|
ENSP00000325831.3:n.*564G=
|
|
ENST00000333684.9:c.696-186G=
|
ENSP00000328814.6:n.696-186G=
|
|
ENST00000352909.7:c.875G=
|
ENSP00000325951.3:p.Gly292=
|
|
ENST00000381168.7:c.*595G=
|
ENSP00000370560.3:n.*595G=
|
|
ENST00000381175.5:c.956G=
|
ENSP00000370567.1:p.Gly319=
|
|
ENST00000381178.5:c.968G=
|
ENSP00000370571.1:p.Gly323=
|
|
ENST00000412076.1:c.136-186G=
|
|
|
ENST00000416223.5:c.169G=
|
|
|
ENST00000461172.1:n.40G=
|
|
|
ENST00000479437.5:n.424G=
|
|
|
NM_000360.3:c.875G=
|
NP_000351.2:p.Gly292=
|
|
NM_199292.2:c.968G=
|
NP_954986.2:p.Gly323=
|
|
NM_199293.2:c.956G=
|
NP_954987.2:p.Gly319=
|
|
XM_011520335.1:c.887G=
|
XP_011518637.1:p.Gly296=
|
|
XM_011520335.2:c.887G=
|
XP_011518637.1:p.Gly296=
|
|
NM_000360.4:c.875G=
MANE Select
|
NP_000351.2:p.Gly292=
|
|
NM_199292.3:c.968G=
|
NP_954986.2:p.Gly323=
|
|
NM_199293.3:c.956G=
|
NP_954987.2:p.Gly319=
|
|