ENST00000682568.1:n.1804A>G
|
|
|
ENST00000682617.1:c.1864A>G
|
ENSP00000507912.1:p.Arg622Gly
|
|
ENST00000682826.1:c.*1040A>G
|
ENSP00000507274.1:n.*1040A>G
|
|
ENST00000682909.1:n.3766A>G
|
|
|
ENST00000683277.1:n.3371A>G
|
|
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ENST00000683407.1:n.1734A>G
|
|
|
ENST00000683962.1:c.*1420A>G
|
ENSP00000506854.1:n.*1420A>G
|
|
ENST00000311895.8:c.1726A>G
MANE Select
|
ENSP00000310520.7:p.Arg576Gly
|
|
ENST00000311895.7:c.1726A>G
|
ENSP00000310520.7:p.Arg576Gly
|
|
ENST00000389138.7:n.1003A>G
|
|
|
NM_005236.2:c.1726A>G , LRG_463t1:c.1726A>G
|
NP_005227.1:p.Arg576Gly
|
|
XM_011522424.1:c.1864A>G
|
XP_011520726.1:p.Arg622Gly
|
|
XM_011522425.1:c.1183A>G
|
XP_011520727.1:p.Arg395Gly
|
|
XM_011522426.1:c.937A>G
|
XP_011520728.1:p.Arg313Gly
|
|
XM_011522427.1:c.376A>G
|
XP_011520729.1:p.Arg126Gly
|
|
XR_932805.1:n.1885A>G
|
|
|
XM_011522424.3:c.1864A>G
|
XP_011520726.1:p.Arg622Gly
|
|
XM_017023043.2:c.937A>G
|
XP_016878532.1:p.Arg313Gly
|
|
NM_005236.3:c.1726A>G
MANE Select
|
NP_005227.1:p.Arg576Gly
|
|