ENST00000682266.1:c.997T>G
|
ENSP00000507766.1:p.Tyr333Asp
|
|
ENST00000682341.1:c.1405T>G
|
ENSP00000508251.1:p.Tyr469Asp
|
|
ENST00000683197.1:c.1405T>G
|
ENSP00000507641.1:p.Tyr469Asp
|
|
ENST00000683411.1:c.997T>G
|
ENSP00000508397.1:p.Tyr333Asp
|
|
ENST00000683437.1:c.997T>G
|
ENSP00000508408.1:p.Tyr333Asp
|
|
ENST00000683613.1:n.2441T>G
|
|
|
ENST00000684663.1:c.1402T>G
|
ENSP00000508009.1:p.Tyr468Asp
|
|
ENST00000324559.9:c.1447T>G
MANE Select
|
ENSP00000315371.9:p.Tyr483Asp
|
|
ENST00000648804.1:n.1782T>G
|
|
|
ENST00000324559.8:c.1447T>G
|
ENSP00000315371.8:p.Tyr483Asp
|
|
NM_001142649.1:c.1444T>G
|
NP_001136121.1:p.Tyr482Asp
|
|
NM_213599.2:c.1447T>G , LRG_868t1:c.1447T>G
|
NP_998764.1:p.Tyr483Asp
|
|
XM_005252820.2:c.1405T>G
|
XP_005252877.2:p.Tyr469Asp
|
|
XM_005252821.2:c.1402T>G
|
XP_005252878.2:p.Tyr468Asp
|
|
XM_005252822.3:c.1369T>G
|
XP_005252879.1:p.Tyr457Asp
|
|
XM_005252823.3:c.1366T>G
|
XP_005252880.1:p.Tyr456Asp
|
|
XM_011519949.1:c.1354T>G
|
XP_011518251.1:p.Tyr452Asp
|
|
XM_005252820.3:c.1405T>G
|
XP_005252877.2:p.Tyr469Asp
|
|
XM_005252821.3:c.1402T>G
|
XP_005252878.2:p.Tyr468Asp
|
|
XM_005252822.4:c.1369T>G
|
XP_005252879.1:p.Tyr457Asp
|
|
XM_011519949.2:c.1354T>G
|
XP_011518251.1:p.Tyr452Asp
|
|
NM_001142649.2:c.1444T>G
|
NP_001136121.1:p.Tyr482Asp
|
|
NM_213599.3:c.1447T>G
MANE Select
|
NP_998764.1:p.Tyr483Asp
|
|