ENST00000698724.1:n.1811T>A
|
|
|
ENST00000698725.1:n.1564T>A
|
|
|
ENST00000698726.1:n.3124T>A
|
|
|
ENST00000698727.1:n.2857T>A
|
|
|
ENST00000698728.1:n.3473T>A
|
|
|
ENST00000698729.1:n.4921T>A
|
|
|
ENST00000698730.1:n.5019T>A
|
|
|
ENST00000698731.1:c.3753T>A
|
ENSP00000513898.1:p.Gly1251=
|
|
ENST00000698732.1:c.*2583T>A
|
ENSP00000513899.1:n.*2583T>A
|
|
ENST00000698733.1:c.*3081T>A
|
ENSP00000513900.1:n.*3081T>A
|
|
ENST00000698734.1:c.*2067T>A
|
ENSP00000513901.1:n.*2067T>A
|
|
ENST00000698735.1:n.4245T>A
|
|
|
ENST00000698736.1:n.4658T>A
|
|
|
ENST00000698737.1:n.4009T>A
|
|
|
ENST00000372371.8:c.3894T>A
MANE Select
|
ENSP00000361446.3:p.Gly1298=
|
|
ENST00000372371.7:c.3894T>A
|
ENSP00000361446.3:p.Gly1298=
|
|
ENST00000616246.4:c.342T>A
|
ENSP00000483738.1:p.Gly114=
|
|
NM_007055.3:c.3894T>A
|
NP_008986.2:p.Gly1298=
|
|
NM_007055.4:c.3894T>A
MANE Select
|
NP_008986.2:p.Gly1298=
|
|