ENST00000228284.8:c.1921C>G
|
ENSP00000228284.4:p.Arg641Gly
|
|
ENST00000546815.6:c.1867C>G
MANE Select
|
ENSP00000449386.2:p.Arg623Gly
|
|
ENST00000651280.1:c.*1023C>G
|
ENSP00000498612.1:n.*1023C>G
|
|
ENST00000228284.7:c.1867C>G
|
ENSP00000228284.3:p.Arg623Gly
|
|
ENST00000431469.6:c.1759C>G
|
ENSP00000414453.2:p.Arg587Gly
|
|
ENST00000546728.5:c.*761C>G
|
ENSP00000449743.1:n.*761C>G
|
|
ENST00000546815.5:c.1921C>G
|
ENSP00000449386.1:p.Arg641Gly
|
|
NM_014706.3:c.1867C>G
|
NP_055521.1:p.Arg623Gly
|
|
XM_005269241.3:c.1921C>G
|
XP_005269298.1:p.Arg641Gly
|
|
XM_011539026.1:c.1003C>G
|
XP_011537328.1:p.Arg335Gly
|
|
NM_014706.4:c.1867C>G
MANE Select
|
NP_055521.1:p.Arg623Gly
|
|
XM_005269241.5:c.1921C>G
|
XP_005269298.1:p.Arg641Gly
|
|
XM_024449284.1:c.1003C>G
|
XP_024305052.1:p.Arg335Gly
|
|