ENST00000682617.1:c.2153C>G
|
ENSP00000507912.1:p.Ala718Gly
|
|
ENST00000683962.1:c.*1709C>G
|
ENSP00000506854.1:n.*1709C>G
|
|
ENST00000311895.8:c.2015C>G
MANE Select
|
ENSP00000310520.7:p.Ala672Gly
|
|
ENST00000311895.7:c.2015C>G
|
ENSP00000310520.7:p.Ala672Gly
|
|
ENST00000389138.7:n.1292C>G
|
|
|
ENST00000462862.1:c.328C>G
|
ENSP00000461322.1:n.328C>G
|
|
NM_005236.2:c.2015C>G , LRG_463t1:c.2015C>G
|
NP_005227.1:p.Ala672Gly
|
|
XM_011522424.1:c.2153C>G
|
XP_011520726.1:p.Ala718Gly
|
|
XM_011522425.1:c.1472C>G
|
XP_011520727.1:p.Ala491Gly
|
|
XM_011522426.1:c.1226C>G
|
XP_011520728.1:p.Ala409Gly
|
|
XM_011522427.1:c.665C>G
|
XP_011520729.1:p.Ala222Gly
|
|
XR_932805.1:n.2174C>G
|
|
|
XM_011522424.3:c.2153C>G
|
XP_011520726.1:p.Ala718Gly
|
|
XM_017023043.2:c.1226C>G
|
XP_016878532.1:p.Ala409Gly
|
|
NM_005236.3:c.2015C>G
MANE Select
|
NP_005227.1:p.Ala672Gly
|
|