ENST00000465011.2:c.*1091G>T
|
ENSP00000419009.1:n.*1091G>T
|
|
ENST00000467655.2:c.*543G>T
|
ENSP00000418547.2:n.*543G>T
|
|
ENST00000704365.1:c.1456G>T
|
ENSP00000515873.1:p.Glu486Ter
|
|
ENST00000704366.1:c.1354G>T
|
ENSP00000515874.1:p.Glu452Ter
|
|
ENST00000704367.1:c.1177G>T
|
ENSP00000515875.1:p.Glu393Ter
|
|
ENST00000704368.1:n.1949G>T
|
|
|
ENST00000704369.1:c.970G>T
|
ENSP00000515876.1:p.Glu324Ter
|
|
ENST00000704370.1:c.1450G>T
|
ENSP00000515877.1:p.Glu484Ter
|
|
ENST00000704372.1:n.1810G>T
|
|
|
ENST00000704444.1:c.1240G>T
|
ENSP00000515896.1:p.Glu414Ter
|
|
ENST00000704445.1:c.1108G>T
|
ENSP00000515897.1:p.Glu370Ter
|
|
ENST00000704446.1:c.1048+866G>T
|
ENSP00000515898.1:n.1048+866G>T
|
|
ENST00000341893.8:c.1456G>T
MANE Select
|
ENSP00000342510.3:p.Glu486Ter
|
|
ENST00000341893.7:c.1456G>T
|
ENSP00000342510.3:p.Glu486Ter
|
|
ENST00000467655.1:c.1071G>T
|
ENSP00000418547.1:n.1071G>T
|
|
ENST00000489172.5:n.1438G>T
|
|
|
ENST00000494050.5:c.1279G>T
|
ENSP00000418185.1:p.Glu427Ter
|
|
NM_001303401.1:c.1279G>T
|
NP_001290330.1:p.Glu427Ter
|
|
NM_024548.3:c.1456G>T
|
NP_078824.2:p.Glu486Ter
|
|
XM_006713743.2:c.1354G>T
|
XP_006713806.1:p.Glu452Ter
|
|
XM_011513125.1:c.1240G>T
|
XP_011511427.1:p.Glu414Ter
|
|
XM_011513126.1:c.1240G>T
|
XP_011511428.1:p.Glu414Ter
|
|
XM_011513127.1:c.1108G>T
|
XP_011511429.1:p.Glu370Ter
|
|
XM_006713743.4:c.1354G>T
|
XP_006713806.1:p.Glu452Ter
|
|
XM_017007178.2:c.1177G>T
|
XP_016862667.1:p.Glu393Ter
|
|
NM_024548.4:c.1456G>T
MANE Select
|
NP_078824.2:p.Glu486Ter
|
|
NM_001303401.2:c.1279G>T
|
NP_001290330.1:p.Glu427Ter
|
|