ENST00000698727.1:n.1268G>A
|
|
|
ENST00000698728.1:n.1787G>A
|
|
|
ENST00000698729.1:n.3333G>A
|
|
|
ENST00000698730.1:n.3333G>A
|
|
|
ENST00000698731.1:c.2067G>A
|
ENSP00000513898.1:p.Leu689=
|
|
ENST00000698732.1:c.*1069G>A
|
ENSP00000513899.1:n.*1069G>A
|
|
ENST00000698733.1:c.*1395G>A
|
ENSP00000513900.1:n.*1395G>A
|
|
ENST00000698734.1:c.2208G>A
|
ENSP00000513901.1:p.Leu736=
|
|
ENST00000698735.1:n.2323G>A
|
|
|
ENST00000698736.1:n.2323G>A
|
|
|
ENST00000698737.1:n.2323G>A
|
|
|
ENST00000698738.1:n.2323G>A
|
|
|
ENST00000698739.1:n.2323G>A
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|
|
ENST00000372371.8:c.2208G>A
MANE Select
|
ENSP00000361446.3:p.Leu736=
|
|
ENST00000372371.7:c.2208G>A
|
ENSP00000361446.3:p.Leu736=
|
|
ENST00000472014.5:n.430G>A
|
|
|
ENST00000473588.2:c.871G>A
|
|
|
NM_007055.3:c.2208G>A
|
NP_008986.2:p.Leu736=
|
|
NM_007055.4:c.2208G>A
MANE Select
|
NP_008986.2:p.Leu736=
|
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