ENST00000546609.2:n.541T>G
|
|
|
ENST00000713544.1:c.710T>G
|
ENSP00000518840.1:p.Leu237Arg
|
|
ENST00000713545.1:c.687T>G
|
ENSP00000518841.1:p.Pro229=
|
|
ENST00000228606.9:c.629T>G
MANE Select
|
ENSP00000228606.4:p.Leu210Arg
|
|
ENST00000228606.8:c.629T>G
|
ENSP00000228606.4:p.Leu210Arg
|
|
ENST00000546567.5:c.-77T>G
|
ENSP00000449472.1:n.-77T>G
|
|
ENST00000546609.1:c.541T>G
|
|
|
ENST00000547344.5:n.768T>G
|
|
|
ENST00000547451.1:n.429T>G
|
|
|
NM_000785.3:c.629T>G
|
NP_000776.1:p.Leu210Arg
|
|
NM_000785.4:c.629T>G
MANE Select
|
NP_000776.1:p.Leu210Arg
|
|