|
ENST00000690509.1:c.*45+10542G>A
(CLCC1)
|
ENSP00000510142.1:n.*45+10542G>A
|
|
|
ENST00000264126.9:c.1684C>T
(GPSM2)
MANE Select
|
ENSP00000264126.3:p.Gln562Ter
|
|
|
ENST00000357393.6:c.-1+39278G>A
(AKNAD1)
|
ENSP00000349968.6:n.-1+39278G>A
|
|
|
ENST00000441735.2:c.1684C>T
(GPSM2)
|
ENSP00000390629.2:p.Gln562Ter
|
|
|
ENST00000446797.2:c.1684C>T
(GPSM2)
|
ENSP00000392138.2:p.Gln562Ter
|
|
|
ENST00000642355.1:c.1684C>T
(GPSM2)
|
ENSP00000496104.1:p.Gln562Ter
|
|
|
ENST00000643643.1:c.773C>T
(GPSM2)
|
|
|
|
ENST00000645164.2:c.1684C>T
(GPSM2)
|
ENSP00000496756.2:p.Gln562Ter
|
|
|
ENST00000674700.1:c.1543+1507C>T
(GPSM2)
|
ENSP00000501743.1:n.1543+1507C>T
|
|
|
ENST00000674731.1:c.*401C>T
(GPSM2)
|
ENSP00000502401.1:n.*401C>T
|
|
|
ENST00000674914.1:c.1735C>T
(GPSM2)
|
ENSP00000501579.1:p.Gln579Ter
|
|
|
ENST00000675086.1:c.1507C>T
(GPSM2)
|
ENSP00000502476.1:p.Gln503Ter
|
|
|
ENST00000675087.1:c.1735C>T
(GPSM2)
|
ENSP00000502020.1:p.Gln579Ter
|
|
|
ENST00000675740.1:n.1299C>T
(GPSM2)
|
|
|
|
ENST00000676184.1:c.1684C>T
(GPSM2)
|
ENSP00000502178.1:p.Gln562Ter
|
|
|
ENST00000676404.1:c.*590C>T
(GPSM2)
|
ENSP00000502346.1:n.*590C>T
|
|
|
ENST00000264126.7:c.1684C>T
(GPSM2)
|
ENSP00000264126.3:p.Gln562Ter
|
|
|
ENST00000357393.5:c.114+39278G>A
|
ENSP00000349968.5:n.114+39278G>A
|
|
|
ENST00000406462.6:c.1684C>T
(GPSM2)
|
ENSP00000385510.1:p.Gln562Ter
|
|
|
ENST00000441735.1:c.453C>T
(GPSM2)
|
|
|
|
NM_013296.4:c.1684C>T
(GPSM2)
|
NP_037428.3:p.Gln562Ter
|
|
|
XM_005270787.2:c.1684C>T
(GPSM2)
|
XP_005270844.1:p.Gln562Ter
|
|
|
XM_006710589.1:c.1627C>T
(GPSM2)
|
XP_006710652.1:p.Gln543Ter
|
|
|
XM_011541301.1:c.1684C>T
(GPSM2)
|
XP_011539603.1:p.Gln562Ter
|
|
|
XM_011541302.1:c.1684C>T
(GPSM2)
|
XP_011539604.1:p.Gln562Ter
|
|
|
NM_001321038.1:c.1684C>T
(GPSM2)
|
NP_001307967.1:p.Gln562Ter
|
|
|
NM_001321039.1:c.1684C>T
(GPSM2)
|
NP_001307968.1:p.Gln562Ter
|
|
|
XM_006710589.3:c.1627C>T
(GPSM2)
|
XP_006710652.1:p.Gln543Ter
|
|
|
XM_011541301.2:c.1684C>T
(GPSM2)
|
XP_011539603.1:p.Gln562Ter
|
|
|
XM_011541302.3:c.1684C>T
(GPSM2)
|
XP_011539604.1:p.Gln562Ter
|
|
|
XM_017001097.2:c.1684C>T
(GPSM2)
|
XP_016856586.1:p.Gln562Ter
|
|
|
XM_017001098.2:c.1684C>T
(GPSM2)
|
XP_016856587.1:p.Gln562Ter
|
|
|
NM_013296.5:c.1684C>T
(GPSM2)
MANE Select
|
NP_037428.3:p.Gln562Ter
|
|
|
NM_001321038.2:c.1684C>T
(GPSM2)
|
NP_001307967.1:p.Gln562Ter
|
|
|
NM_001321039.2:c.1684C>T
(GPSM2)
|
NP_001307968.1:p.Gln562Ter
|
|
|
NM_001321039.3:c.1684C>T
(GPSM2)
|
NP_001307968.1:p.Gln562Ter
|
|
