ENST00000465011.2:c.*1143T>C
|
ENSP00000419009.1:n.*1143T>C
|
|
ENST00000467655.2:c.*595T>C
|
ENSP00000418547.2:n.*595T>C
|
|
ENST00000704365.1:c.1508T>C
|
ENSP00000515873.1:p.Phe503Ser
|
|
ENST00000704366.1:c.1406T>C
|
ENSP00000515874.1:p.Phe469Ser
|
|
ENST00000704367.1:c.1229T>C
|
ENSP00000515875.1:p.Phe410Ser
|
|
ENST00000704368.1:n.2001T>C
|
|
|
ENST00000704369.1:c.1022T>C
|
ENSP00000515876.1:p.Phe341Ser
|
|
ENST00000704370.1:c.1502T>C
|
ENSP00000515877.1:p.Phe501Ser
|
|
ENST00000704372.1:n.1862T>C
|
|
|
ENST00000704444.1:c.1292T>C
|
ENSP00000515896.1:p.Phe431Ser
|
|
ENST00000704445.1:c.1160T>C
|
ENSP00000515897.1:p.Phe387Ser
|
|
ENST00000704446.1:c.1048+918T>C
|
ENSP00000515898.1:n.1048+918T>C
|
|
ENST00000341893.8:c.1508T>C
MANE Select
|
ENSP00000342510.3:p.Phe503Ser
|
|
ENST00000341893.7:c.1508T>C
|
ENSP00000342510.3:p.Phe503Ser
|
|
ENST00000467655.1:c.1123T>C
|
ENSP00000418547.1:n.1123T>C
|
|
ENST00000489172.5:n.1490T>C
|
|
|
ENST00000494050.5:c.1331T>C
|
ENSP00000418185.1:p.Phe444Ser
|
|
NM_001303401.1:c.1331T>C
|
NP_001290330.1:p.Phe444Ser
|
|
NM_024548.3:c.1508T>C
|
NP_078824.2:p.Phe503Ser
|
|
XM_006713743.2:c.1406T>C
|
XP_006713806.1:p.Phe469Ser
|
|
XM_011513125.1:c.1292T>C
|
XP_011511427.1:p.Phe431Ser
|
|
XM_011513126.1:c.1292T>C
|
XP_011511428.1:p.Phe431Ser
|
|
XM_011513127.1:c.1160T>C
|
XP_011511429.1:p.Phe387Ser
|
|
XM_006713743.4:c.1406T>C
|
XP_006713806.1:p.Phe469Ser
|
|
XM_017007178.2:c.1229T>C
|
XP_016862667.1:p.Phe410Ser
|
|
NM_024548.4:c.1508T>C
MANE Select
|
NP_078824.2:p.Phe503Ser
|
|
NM_001303401.2:c.1331T>C
|
NP_001290330.1:p.Phe444Ser
|
|