ENST00000593767.3:c.1727C>G
|
ENSP00000470692.3:p.Ala576Gly
|
|
ENST00000312865.10:c.1727C>G
MANE Select
|
ENSP00000326767.5:p.Ala576Gly
|
|
ENST00000538643.5:c.1088C>G
|
ENSP00000437496.1:p.Ala363Gly
|
|
ENST00000593767.1:c.173C>G
|
|
|
ENST00000594998.1:n.2347C>G
|
|
|
ENST00000595185.5:c.689-1305C>G
|
ENSP00000470027.1:n.689-1305C>G
|
|
ENST00000612791.4:c.762-1253C>G
|
ENSP00000479851.1:n.762-1253C>G
|
|
ENST00000612854.4:c.451-667C>G
|
ENSP00000482155.1:n.451-667C>G
|
|
ENST00000617849.4:c.932C>G
|
ENSP00000484882.1:p.Ala311Gly
|
|
ENST00000618715.4:c.932C>G
|
ENSP00000480731.1:p.Ala311Gly
|
|
ENST00000620467.4:c.973-697C>G
|
ENSP00000482659.1:n.973-697C>G
|
|
ENST00000622046.1:c.194C>G
|
ENSP00000483584.1:p.Ala65Gly
|
|
ENST00000622402.4:c.146-241C>G
|
ENSP00000478074.1:n.146-241C>G
|
|
NM_030973.3:c.1727C>G , LRG_368t1:c.1727C>G
|
NP_112235.2:p.Ala576Gly
|
|
XM_011527353.1:c.1727C>G
|
XP_011525655.1:p.Ala576Gly
|
|
NM_001378355.1:c.1727C>G
|
NP_001365284.1:p.Ala576Gly
|
|
NM_030973.4:c.1727C>G
MANE Select
|
NP_112235.2:p.Ala576Gly
|
|