ENST00000698724.1:n.1820G>T
|
|
|
ENST00000698725.1:n.1573G>T
|
|
|
ENST00000698726.1:n.3133G>T
|
|
|
ENST00000698727.1:n.2866G>T
|
|
|
ENST00000698728.1:n.3482G>T
|
|
|
ENST00000698729.1:n.4930G>T
|
|
|
ENST00000698730.1:n.5028G>T
|
|
|
ENST00000698731.1:c.3762G>T
|
ENSP00000513898.1:p.Leu1254=
|
|
ENST00000698732.1:c.*2592G>T
|
ENSP00000513899.1:n.*2592G>T
|
|
ENST00000698733.1:c.*3090G>T
|
ENSP00000513900.1:n.*3090G>T
|
|
ENST00000698734.1:c.*2076G>T
|
ENSP00000513901.1:n.*2076G>T
|
|
ENST00000698735.1:n.4254G>T
|
|
|
ENST00000698736.1:n.4667G>T
|
|
|
ENST00000698737.1:n.4018G>T
|
|
|
ENST00000372371.8:c.3903G>T
MANE Select
|
ENSP00000361446.3:p.Leu1301=
|
|
ENST00000372371.7:c.3903G>T
|
ENSP00000361446.3:p.Leu1301=
|
|
ENST00000616246.4:c.351G>T
|
ENSP00000483738.1:p.Leu117=
|
|
NM_007055.3:c.3903G>T
|
NP_008986.2:p.Leu1301=
|
|
NM_007055.4:c.3903G>T
MANE Select
|
NP_008986.2:p.Leu1301=
|
|