ENST00000467236.2:n.462G>C
|
|
|
ENST00000699980.1:n.1226G>C
|
|
|
ENST00000369980.8:c.1682G>C
MANE Select
|
ENSP00000358997.3:p.Trp561Ser
|
|
ENST00000369973.7:c.*625G>C
|
ENSP00000358990.3:n.*625G>C
|
|
ENST00000369974.6:c.1445G>C
|
ENSP00000358991.2:p.Trp482Ser
|
|
ENST00000369980.7:c.1682G>C
|
ENSP00000358997.3:p.Trp561Ser
|
|
ENST00000393687.6:c.1592G>C
|
ENSP00000377291.2:p.Trp531Ser
|
|
ENST00000429936.6:c.1670G>C
|
ENSP00000392662.2:p.Trp557Ser
|
|
ENST00000437278.5:c.373G>C
|
|
|
ENST00000443220.1:c.927G>C
|
|
|
ENST00000444230.5:c.529-2175G>C
|
ENSP00000399974.1:n.529-2175G>C
|
|
ENST00000444254.1:c.348G>C
|
|
|
ENST00000455690.5:c.280-613G>C
|
ENSP00000411809.1:n.280-613G>C
|
|
ENST00000477274.1:n.616-2480G>C
|
|
|
NM_001025242.1:c.1592G>C
|
NP_001020413.1:p.Trp531Ser
|
|
NM_001025243.1:c.1445G>C
|
NP_001020414.1:p.Trp482Ser
|
|
NM_001569.3:c.1682G>C
|
NP_001560.2:p.Trp561Ser
|
|
XM_005274668.2:c.1670G>C
|
XP_005274725.1:p.Trp557Ser
|
|
XM_011531158.1:c.1355G>C
|
XP_011529460.1:p.Trp452Ser
|
|
XM_005274668.4:c.1670G>C
|
XP_005274725.1:p.Trp557Ser
|
|
NM_001569.4:c.1682G>C
MANE Select
|
NP_001560.2:p.Trp561Ser
|
|
NM_001025242.2:c.1592G>C
|
NP_001020413.1:p.Trp531Ser
|
|
NM_001025243.2:c.1445G>C
|
NP_001020414.1:p.Trp482Ser
|
|