ENST00000698727.1:n.1595T>G
|
|
|
ENST00000698728.1:n.2114T>G
|
|
|
ENST00000698729.1:n.3660T>G
|
|
|
ENST00000698730.1:n.3660T>G
|
|
|
ENST00000698731.1:c.2394T>G
|
ENSP00000513898.1:p.Thr798=
|
|
ENST00000698732.1:c.*1396T>G
|
ENSP00000513899.1:n.*1396T>G
|
|
ENST00000698733.1:c.*1722T>G
|
ENSP00000513900.1:n.*1722T>G
|
|
ENST00000698734.1:c.2535T>G
|
ENSP00000513901.1:p.Thr845=
|
|
ENST00000698735.1:n.2650T>G
|
|
|
ENST00000698736.1:n.2650T>G
|
|
|
ENST00000698737.1:n.2650T>G
|
|
|
ENST00000698738.1:n.2650T>G
|
|
|
ENST00000698739.1:n.2650T>G
|
|
|
ENST00000372371.8:c.2535T>G
MANE Select
|
ENSP00000361446.3:p.Thr845=
|
|
ENST00000372371.7:c.2535T>G
|
ENSP00000361446.3:p.Thr845=
|
|
ENST00000472014.5:n.469+4654T>G
|
|
|
NM_007055.3:c.2535T>G
|
NP_008986.2:p.Thr845=
|
|
NM_007055.4:c.2535T>G
MANE Select
|
NP_008986.2:p.Thr845=
|
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