ENST00000698727.1:n.1164G>T
|
|
|
ENST00000698728.1:n.1683G>T
|
|
|
ENST00000698729.1:n.3229G>T
|
|
|
ENST00000698730.1:n.3229G>T
|
|
|
ENST00000698731.1:c.1963G>T
|
ENSP00000513898.1:p.Asp655Tyr
|
|
ENST00000698732.1:c.*965G>T
|
ENSP00000513899.1:n.*965G>T
|
|
ENST00000698733.1:c.*1291G>T
|
ENSP00000513900.1:n.*1291G>T
|
|
ENST00000698734.1:c.2104G>T
|
ENSP00000513901.1:p.Asp702Tyr
|
|
ENST00000698735.1:n.2219G>T
|
|
|
ENST00000698736.1:n.2219G>T
|
|
|
ENST00000698737.1:n.2219G>T
|
|
|
ENST00000698738.1:n.2219G>T
|
|
|
ENST00000698739.1:n.2219G>T
|
|
|
ENST00000372371.8:c.2104G>T
MANE Select
|
ENSP00000361446.3:p.Asp702Tyr
|
|
ENST00000372371.7:c.2104G>T
|
ENSP00000361446.3:p.Asp702Tyr
|
|
ENST00000472014.5:n.326G>T
|
|
|
ENST00000473588.2:c.767G>T
|
|
|
NM_007055.3:c.2104G>T
|
NP_008986.2:p.Asp702Tyr
|
|
NM_007055.4:c.2104G>T
MANE Select
|
NP_008986.2:p.Asp702Tyr
|
|