ENST00000682568.1:n.1616G>C
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|
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ENST00000682617.1:c.1676G>C
|
ENSP00000507912.1:p.Gly559Ala
|
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ENST00000682826.1:c.*852G>C
|
ENSP00000507274.1:n.*852G>C
|
|
ENST00000682909.1:n.3578G>C
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|
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ENST00000683277.1:n.3183G>C
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ENST00000683407.1:n.1546G>C
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ENST00000683962.1:c.*1232G>C
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ENSP00000506854.1:n.*1232G>C
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|
ENST00000311895.8:c.1538G>C
MANE Select
|
ENSP00000310520.7:p.Gly513Ala
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ENST00000311895.7:c.1538G>C
|
ENSP00000310520.7:p.Gly513Ala
|
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ENST00000389138.7:n.815G>C
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|
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NM_005236.2:c.1538G>C , LRG_463t1:c.1538G>C
|
NP_005227.1:p.Gly513Ala
|
|
XM_011522424.1:c.1676G>C
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XP_011520726.1:p.Gly559Ala
|
|
XM_011522425.1:c.995G>C
|
XP_011520727.1:p.Gly332Ala
|
|
XM_011522426.1:c.749G>C
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XP_011520728.1:p.Gly250Ala
|
|
XM_011522427.1:c.188G>C
|
XP_011520729.1:p.Gly63Ala
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|
XR_932805.1:n.1697G>C
|
|
|
XM_011522424.3:c.1676G>C
|
XP_011520726.1:p.Gly559Ala
|
|
XM_017023043.2:c.749G>C
|
XP_016878532.1:p.Gly250Ala
|
|
NM_005236.3:c.1538G>C
MANE Select
|
NP_005227.1:p.Gly513Ala
|
|