ENST00000625662.3:c.2215G>A
|
|
|
ENST00000628118.2:c.1742G>A
|
|
|
ENST00000700551.1:c.*1539G>A
|
ENSP00000515057.1:n.*1539G>A
|
|
ENST00000394196.9:c.2708G>A
MANE Select
|
ENSP00000377747.4:p.Arg903Lys
|
|
ENST00000635856.1:n.3280G>A
|
|
|
ENST00000636306.1:n.268G>A
|
|
|
ENST00000636881.1:c.2079G>A
|
|
|
ENST00000637572.1:n.3452G>A
|
|
|
ENST00000394196.8:c.2708G>A
|
ENSP00000377747.4:p.Arg903Lys
|
|
ENST00000625463.1:c.248G>A
|
ENSP00000486391.1:p.Arg83Lys
|
|
ENST00000626874.2:c.2708G>A
|
ENSP00000486629.1:p.Arg903Lys
|
|
ENST00000628118.1:n.487G>A
|
|
|
NM_001271.3:c.2708G>A
|
NP_001262.3:p.Arg903Lys
|
|
NM_001271.4:c.2708G>A
MANE Select
|
NP_001262.3:p.Arg903Lys
|
|