ENST00000546609.2:n.639C>G
|
|
|
ENST00000713544.1:c.808C>G
|
ENSP00000518840.1:p.Arg270Gly
|
|
ENST00000713545.1:c.785C>G
|
ENSP00000518841.1:p.Ala262Gly
|
|
ENST00000228606.9:c.727C>G
MANE Select
|
ENSP00000228606.4:p.Arg243Gly
|
|
ENST00000228606.8:c.727C>G
|
ENSP00000228606.4:p.Arg243Gly
|
|
ENST00000546567.5:c.22C>G
|
ENSP00000449472.1:p.Arg8Gly
|
|
ENST00000546609.1:c.639C>G
|
|
|
ENST00000547344.5:n.866C>G
|
|
|
ENST00000547451.1:n.527C>G
|
|
|
NM_000785.3:c.727C>G
|
NP_000776.1:p.Arg243Gly
|
|
NM_000785.4:c.727C>G
MANE Select
|
NP_000776.1:p.Arg243Gly
|
|