ENST00000465011.2:c.*1117G>T
|
ENSP00000419009.1:n.*1117G>T
|
|
ENST00000467655.2:c.*569G>T
|
ENSP00000418547.2:n.*569G>T
|
|
ENST00000704365.1:c.1482G>T
|
ENSP00000515873.1:p.Leu494Phe
|
|
ENST00000704366.1:c.1380G>T
|
ENSP00000515874.1:p.Leu460Phe
|
|
ENST00000704367.1:c.1203G>T
|
ENSP00000515875.1:p.Leu401Phe
|
|
ENST00000704368.1:n.1975G>T
|
|
|
ENST00000704369.1:c.996G>T
|
ENSP00000515876.1:p.Leu332Phe
|
|
ENST00000704370.1:c.1476G>T
|
ENSP00000515877.1:p.Leu492Phe
|
|
ENST00000704372.1:n.1836G>T
|
|
|
ENST00000704444.1:c.1266G>T
|
ENSP00000515896.1:p.Leu422Phe
|
|
ENST00000704445.1:c.1134G>T
|
ENSP00000515897.1:p.Leu378Phe
|
|
ENST00000704446.1:c.1048+892G>T
|
ENSP00000515898.1:n.1048+892G>T
|
|
ENST00000341893.8:c.1482G>T
MANE Select
|
ENSP00000342510.3:p.Leu494Phe
|
|
ENST00000341893.7:c.1482G>T
|
ENSP00000342510.3:p.Leu494Phe
|
|
ENST00000467655.1:c.1097G>T
|
ENSP00000418547.1:n.1097G>T
|
|
ENST00000489172.5:n.1464G>T
|
|
|
ENST00000494050.5:c.1305G>T
|
ENSP00000418185.1:p.Leu435Phe
|
|
NM_001303401.1:c.1305G>T
|
NP_001290330.1:p.Leu435Phe
|
|
NM_024548.3:c.1482G>T
|
NP_078824.2:p.Leu494Phe
|
|
XM_006713743.2:c.1380G>T
|
XP_006713806.1:p.Leu460Phe
|
|
XM_011513125.1:c.1266G>T
|
XP_011511427.1:p.Leu422Phe
|
|
XM_011513126.1:c.1266G>T
|
XP_011511428.1:p.Leu422Phe
|
|
XM_011513127.1:c.1134G>T
|
XP_011511429.1:p.Leu378Phe
|
|
XM_006713743.4:c.1380G>T
|
XP_006713806.1:p.Leu460Phe
|
|
XM_017007178.2:c.1203G>T
|
XP_016862667.1:p.Leu401Phe
|
|
NM_024548.4:c.1482G>T
MANE Select
|
NP_078824.2:p.Leu494Phe
|
|
NM_001303401.2:c.1305G>T
|
NP_001290330.1:p.Leu435Phe
|
|