|
ENST00000700029.2:c.770_771delinsAT
|
ENSP00000514759.2:p.Phe257Tyr
|
|
|
ENST00000710265.1:c.770_771delinsAT
|
ENSP00000518161.1:p.Phe257Tyr
|
|
|
ENST00000472832.3:c.770_771delinsAT
|
ENSP00000483066.2:p.Phe257Tyr
|
|
|
ENST00000688158.2:n.1505_1506delinsAT
|
|
|
|
ENST00000688922.2:c.*600_*601delinsAT
|
ENSP00000508742.2:n.*600_*601delinsAT
|
|
|
ENST00000700021.1:c.725_726delinsAT
|
ENSP00000514757.1:p.Phe242Tyr
|
|
|
ENST00000700022.1:c.*109_*110delinsAT
|
ENSP00000514758.1:n.*109_*110delinsAT
|
|
|
ENST00000700023.1:n.1928_1929delinsAT
|
|
|
|
ENST00000700024.1:n.2162_2163delinsAT
|
|
|
|
ENST00000700025.1:n.1539_1540delinsAT
|
|
|
|
ENST00000700026.1:n.407_408delinsAT
|
|
|
|
ENST00000700029.1:c.604_605delinsAT
|
|
|
|
ENST00000706954.1:c.770_771delinsAT
|
ENSP00000516674.1:p.Phe257Tyr
|
|
|
ENST00000706955.1:c.*805_*806delinsAT
|
ENSP00000516675.1:n.*805_*806delinsAT
|
|
|
ENST00000686459.1:c.*356_*357delinsAT
|
ENSP00000508909.1:n.*356_*357delinsAT
|
|
|
ENST00000688158.1:c.*881_*882delinsAT
|
ENSP00000509254.1:n.*881_*882delinsAT
|
|
|
ENST00000688308.1:c.770_771delinsAT
|
ENSP00000508752.1:p.Phe257Tyr
|
|
|
ENST00000688922.1:c.691_692delinsAT
|
|
|
|
ENST00000693560.1:c.1289_1290delinsAT
|
ENSP00000509861.1:p.Phe430Tyr
|
|
|
ENST00000371953.8:c.770_771delinsAT
MANE Select
|
ENSP00000361021.3:p.Phe257Tyr
|
|
|
ENST00000371953.7:c.770_771delinsAT
|
ENSP00000361021.3:p.Phe257Tyr
|
|
|
ENST00000472832.2:c.197_198delinsAT
|
ENSP00000483066.1:p.Phe66Tyr
|
|
|
NM_000314.5:c.770_771delinsAT
|
NP_000305.3:p.Phe257Tyr
|
|
|
NM_000314.6:c.770_771delinsAT
|
NP_000305.3:p.Phe257Tyr
|
|
|
NM_001304717.2:c.1289_1290delinsAT
|
NP_001291646.2:p.Phe430Tyr
|
|
|
NM_001304718.1:c.179_180delinsAT
|
NP_001291647.1:p.Phe60Tyr
|
|
|
XM_006717926.2:c.725_726delinsAT
|
XP_006717989.1:p.Phe242Tyr
|
|
|
XM_011539981.1:c.770_771delinsAT
|
XP_011538283.1:p.Phe257Tyr
|
|
|
XM_011539982.1:c.674_675delinsAT
|
XP_011538284.1:p.Phe225Tyr
|
|
|
XR_945791.1:n.1340_1341delinsAT
|
|
|
|
NM_000314.7:c.770_771delinsAT
|
NP_000305.3:p.Phe257Tyr
|
|
|
NM_001304717.5:c.1289_1290delinsAT
|
NP_001291646.4:p.Phe430Tyr
|
|
|
NM_001304718.2:c.179_180delinsAT
|
NP_001291647.1:p.Phe60Tyr
|
|
|
NM_000314.8:c.770_771delinsAT
MANE Select
|
NP_000305.3:p.Phe257Tyr
|
|
