ENST00000546609.2:n.529G>T
|
|
|
ENST00000713544.1:c.698G>T
|
ENSP00000518840.1:p.Arg233Leu
|
|
ENST00000713545.1:c.675G>T
|
ENSP00000518841.1:p.Ala225=
|
|
ENST00000228606.9:c.617G>T
MANE Select
|
ENSP00000228606.4:p.Arg206Leu
|
|
ENST00000228606.8:c.617G>T
|
ENSP00000228606.4:p.Arg206Leu
|
|
ENST00000546567.5:c.-89G>T
|
ENSP00000449472.1:n.-89G>T
|
|
ENST00000546609.1:c.529G>T
|
|
|
ENST00000547344.5:n.756G>T
|
|
|
ENST00000547451.1:n.417G>T
|
|
|
NM_000785.3:c.617G>T
|
NP_000776.1:p.Arg206Leu
|
|
NM_000785.4:c.617G>T
MANE Select
|
NP_000776.1:p.Arg206Leu
|
|