ENST00000467236.2:n.359G>C
|
|
|
ENST00000699980.1:n.1123G>C
|
|
|
ENST00000369980.8:c.1579G>C
MANE Select
|
ENSP00000358997.3:p.Gly527Arg
|
|
ENST00000369973.7:c.*522G>C
|
ENSP00000358990.3:n.*522G>C
|
|
ENST00000369974.6:c.1342G>C
|
ENSP00000358991.2:p.Gly448Arg
|
|
ENST00000369980.7:c.1579G>C
|
ENSP00000358997.3:p.Gly527Arg
|
|
ENST00000393687.6:c.1540-51G>C
|
ENSP00000377291.2:n.1540-51G>C
|
|
ENST00000429936.6:c.1618-51G>C
|
ENSP00000392662.2:n.1618-51G>C
|
|
ENST00000437278.5:c.321-51G>C
|
|
|
ENST00000443220.1:c.824G>C
|
|
|
ENST00000444230.5:c.529-2278G>C
|
ENSP00000399974.1:n.529-2278G>C
|
|
ENST00000444254.1:c.245G>C
|
|
|
ENST00000455690.5:c.279+648G>C
|
ENSP00000411809.1:n.279+648G>C
|
|
ENST00000467236.1:n.376G>C
|
|
|
ENST00000477274.1:n.616-2583G>C
|
|
|
NM_001025242.1:c.1540-51G>C
|
NP_001020413.1:n.1540-51G>C
|
|
NM_001025243.1:c.1342G>C
|
NP_001020414.1:p.Gly448Arg
|
|
NM_001569.3:c.1579G>C
|
NP_001560.2:p.Gly527Arg
|
|
XM_005274668.2:c.1618-51G>C
|
XP_005274725.1:n.1618-51G>C
|
|
XM_011531158.1:c.1303-51G>C
|
XP_011529460.1:n.1303-51G>C
|
|
XM_005274668.4:c.1618-51G>C
|
XP_005274725.1:n.1618-51G>C
|
|
NM_001569.4:c.1579G>C
MANE Select
|
NP_001560.2:p.Gly527Arg
|
|
NM_001025242.2:c.1540-51G>C
|
NP_001020413.1:n.1540-51G>C
|
|
NM_001025243.2:c.1342G>C
|
NP_001020414.1:p.Gly448Arg
|
|