|
ENST00000700029.2:c.1021G>T
|
ENSP00000514759.2:p.Asp341Tyr
|
|
|
ENST00000710265.1:c.928G>T
|
ENSP00000518161.1:p.Asp310Tyr
|
|
|
ENST00000472832.3:c.928G>T
|
ENSP00000483066.2:p.Asp310Tyr
|
|
|
ENST00000688158.2:n.1663G>T
|
|
|
|
ENST00000688922.2:c.*758G>T
|
ENSP00000508742.2:n.*758G>T
|
|
|
ENST00000700021.1:c.883G>T
|
ENSP00000514757.1:p.Asp295Tyr
|
|
|
ENST00000700022.1:c.*267G>T
|
ENSP00000514758.1:n.*267G>T
|
|
|
ENST00000700023.1:n.2086G>T
|
|
|
|
ENST00000700024.1:n.2320G>T
|
|
|
|
ENST00000700025.1:n.1697G>T
|
|
|
|
ENST00000700026.1:n.565G>T
|
|
|
|
ENST00000706954.1:c.928G>T
|
ENSP00000516674.1:p.Asp310Tyr
|
|
|
ENST00000706955.1:c.*963G>T
|
ENSP00000516675.1:n.*963G>T
|
|
|
ENST00000686459.1:c.*514G>T
|
ENSP00000508909.1:n.*514G>T
|
|
|
ENST00000688158.1:c.*1039G>T
|
ENSP00000509254.1:n.*1039G>T
|
|
|
ENST00000688308.1:c.928G>T
|
ENSP00000508752.1:p.Asp310Tyr
|
|
|
ENST00000688922.1:c.849G>T
|
|
|
|
ENST00000693560.1:c.1447G>T
|
ENSP00000509861.1:p.Asp483Tyr
|
|
|
ENST00000371953.8:c.928G>T
MANE Select
|
ENSP00000361021.3:p.Asp310Tyr
|
|
|
ENST00000371953.7:c.928G>T
|
ENSP00000361021.3:p.Asp310Tyr
|
|
|
ENST00000472832.2:c.355G>T
|
ENSP00000483066.1:p.Asp119Tyr
|
|
|
NM_000314.5:c.928G>T
|
NP_000305.3:p.Asp310Tyr
|
|
|
NM_000314.6:c.928G>T
|
NP_000305.3:p.Asp310Tyr
|
|
|
NM_001304717.2:c.1447G>T
|
NP_001291646.2:p.Asp483Tyr
|
|
|
NM_001304718.1:c.337G>T
|
NP_001291647.1:p.Asp113Tyr
|
|
|
XM_006717926.2:c.883G>T
|
XP_006717989.1:p.Asp295Tyr
|
|
|
XM_011539981.1:c.928G>T
|
XP_011538283.1:p.Asp310Tyr
|
|
|
XM_011539982.1:c.832G>T
|
XP_011538284.1:p.Asp278Tyr
|
|
|
XR_945791.1:n.1498G>T
|
|
|
|
NM_000314.7:c.928G>T
|
NP_000305.3:p.Asp310Tyr
|
|
|
NM_001304717.5:c.1447G>T
|
NP_001291646.4:p.Asp483Tyr
|
|
|
NM_001304718.2:c.337G>T
|
NP_001291647.1:p.Asp113Tyr
|
|
|
NM_000314.8:c.928G>T
MANE Select
|
NP_000305.3:p.Asp310Tyr
|
|
