ENST00000682568.1:n.1613A>G
|
|
|
ENST00000682617.1:c.1673A>G
|
ENSP00000507912.1:p.Glu558Gly
|
|
ENST00000682826.1:c.*849A>G
|
ENSP00000507274.1:n.*849A>G
|
|
ENST00000682909.1:n.3575A>G
|
|
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ENST00000683277.1:n.3180A>G
|
|
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ENST00000683407.1:n.1543A>G
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|
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ENST00000683962.1:c.*1229A>G
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ENSP00000506854.1:n.*1229A>G
|
|
ENST00000311895.8:c.1535A>G
MANE Select
|
ENSP00000310520.7:p.Glu512Gly
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|
ENST00000311895.7:c.1535A>G
|
ENSP00000310520.7:p.Glu512Gly
|
|
ENST00000389138.7:n.812A>G
|
|
|
NM_005236.2:c.1535A>G , LRG_463t1:c.1535A>G
|
NP_005227.1:p.Glu512Gly
|
|
XM_011522424.1:c.1673A>G
|
XP_011520726.1:p.Glu558Gly
|
|
XM_011522425.1:c.992A>G
|
XP_011520727.1:p.Glu331Gly
|
|
XM_011522426.1:c.746A>G
|
XP_011520728.1:p.Glu249Gly
|
|
XM_011522427.1:c.185A>G
|
XP_011520729.1:p.Glu62Gly
|
|
XR_932805.1:n.1694A>G
|
|
|
XM_011522424.3:c.1673A>G
|
XP_011520726.1:p.Glu558Gly
|
|
XM_017023043.2:c.746A>G
|
XP_016878532.1:p.Glu249Gly
|
|
NM_005236.3:c.1535A>G
MANE Select
|
NP_005227.1:p.Glu512Gly
|
|