ENST00000698728.1:n.1223T=
|
|
|
ENST00000698729.1:n.2769T=
|
|
|
ENST00000698730.1:n.2769T=
|
|
|
ENST00000698731.1:c.1503T=
|
ENSP00000513898.1:p.Gly501=
|
|
ENST00000698732.1:c.*505T=
|
ENSP00000513899.1:n.*505T=
|
|
ENST00000698733.1:c.*831T=
|
ENSP00000513900.1:n.*831T=
|
|
ENST00000698734.1:c.1644T=
|
ENSP00000513901.1:p.Gly548=
|
|
ENST00000698735.1:n.1759T=
|
|
|
ENST00000698736.1:n.1759T=
|
|
|
ENST00000698737.1:n.1759T=
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|
|
ENST00000698738.1:n.1759T=
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|
|
ENST00000698739.1:n.1759T=
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|
|
ENST00000372371.8:c.1644T=
MANE Select
|
ENSP00000361446.3:p.Gly548=
|
|
ENST00000372371.7:c.1644T=
|
ENSP00000361446.3:p.Gly548=
|
|
ENST00000473588.2:c.446T=
|
|
|
NM_007055.3:c.1644T=
|
NP_008986.2:p.Gly548=
|
|
NM_007055.4:c.1644T=
MANE Select
|
NP_008986.2:p.Gly548=
|
|