|
ENST00000296137.7:c.1045C>T
MANE Select
|
ENSP00000296137.2:p.Gln349Ter
|
|
|
ENST00000296137.6:c.1045C>T
|
ENSP00000296137.2:p.Gln349Ter
|
|
|
ENST00000535325.5:c.1045C>T
|
ENSP00000441178.1:p.Gln349Ter
|
|
|
NM_024513.3:c.1045C>T
|
NP_078789.2:p.Gln349Ter
|
|
|
XM_006713333.2:c.1045C>T
|
XP_006713396.1:p.Gln349Ter
|
|
|
XM_006713334.2:c.1045C>T
|
XP_006713397.1:p.Gln349Ter
|
|
|
XM_011534111.1:c.1045C>T
|
XP_011532413.1:p.Gln349Ter
|
|
|
XM_011534112.1:c.1045C>T
|
XP_011532414.1:p.Gln349Ter
|
|
|
XR_245157.1:n.1260C>T
|
|
|
|
XM_006713333.3:c.1045C>T
|
XP_006713396.1:p.Gln349Ter
|
|
|
XM_006713334.3:c.1045C>T
|
XP_006713397.1:p.Gln349Ter
|
|
|
XM_011534111.3:c.1045C>T
|
XP_011532413.1:p.Gln349Ter
|
|
|
XR_001740265.1:n.1260C>T
|
|
|
|
NM_024513.4:c.1045C>T
MANE Select
|
NP_078789.2:p.Gln349Ter
|
|
|
NM_001386421.1:c.1045C>T
|
NP_001373350.1:p.Gln349Ter
|
|
|
NM_001386422.1:c.1045C>T
|
NP_001373351.1:p.Gln349Ter
|
|
|
NM_001386423.1:c.1045C>T
|
NP_001373352.1:p.Gln349Ter
|
|
|
NM_001386424.1:c.1045C>T
|
NP_001373353.1:p.Gln349Ter
|
|
|
NM_001386425.1:c.1045C>T
|
NP_001373354.1:p.Gln349Ter
|
|
|
NM_001386426.1:c.925C>T
|
NP_001373355.1:p.Gln309Ter
|
|
|
NM_001386427.1:c.901C>T
|
NP_001373356.1:p.Gln301Ter
|
|
|
NM_001386428.1:c.1045C>T
|
NP_001373357.1:p.Gln349Ter
|
|
|
NM_001386429.1:c.1045C>T
|
NP_001373358.1:p.Gln349Ter
|
|
|
NM_001386430.1:c.445C>T
|
NP_001373359.1:p.Gln149Ter
|
|
|
NR_170107.1:n.1260C>T
|
|
|
