ENST00000352909.8:c.876C>A
MANE Select
|
ENSP00000325951.4:p.Gly292=
|
|
ENST00000324155.8:c.*565C>A
|
ENSP00000325831.3:n.*565C>A
|
|
ENST00000333684.9:c.696-185C>A
|
ENSP00000328814.6:n.696-185C>A
|
|
ENST00000352909.7:c.876C>A
|
ENSP00000325951.3:p.Gly292=
|
|
ENST00000381168.7:c.*596C>A
|
ENSP00000370560.3:n.*596C>A
|
|
ENST00000381175.5:c.957C>A
|
ENSP00000370567.1:p.Gly319=
|
|
ENST00000381178.5:c.969C>A
|
ENSP00000370571.1:p.Gly323=
|
|
ENST00000412076.1:c.136-185C>A
|
|
|
ENST00000416223.5:c.170C>A
|
|
|
ENST00000461172.1:n.41C>A
|
|
|
ENST00000479437.5:n.425C>A
|
|
|
NM_000360.3:c.876C>A
|
NP_000351.2:p.Gly292=
|
|
NM_199292.2:c.969C>A
|
NP_954986.2:p.Gly323=
|
|
NM_199293.2:c.957C>A
|
NP_954987.2:p.Gly319=
|
|
XM_011520335.1:c.888C>A
|
XP_011518637.1:p.Gly296=
|
|
XM_011520335.2:c.888C>A
|
XP_011518637.1:p.Gly296=
|
|
NM_000360.4:c.876C>A
MANE Select
|
NP_000351.2:p.Gly292=
|
|
NM_199292.3:c.969C>A
|
NP_954986.2:p.Gly323=
|
|
NM_199293.3:c.957C>A
|
NP_954987.2:p.Gly319=
|
|