ENST00000682568.1:n.1841T>C
|
|
|
ENST00000682617.1:c.1901T>C
|
ENSP00000507912.1:p.Val634Ala
|
|
ENST00000682826.1:c.*1077T>C
|
ENSP00000507274.1:n.*1077T>C
|
|
ENST00000682909.1:n.3803T>C
|
|
|
ENST00000683277.1:n.3408T>C
|
|
|
ENST00000683407.1:n.1771T>C
|
|
|
ENST00000683962.1:c.*1457T>C
|
ENSP00000506854.1:n.*1457T>C
|
|
ENST00000311895.8:c.1763T>C
MANE Select
|
ENSP00000310520.7:p.Val588Ala
|
|
ENST00000311895.7:c.1763T>C
|
ENSP00000310520.7:p.Val588Ala
|
|
ENST00000389138.7:n.1040T>C
|
|
|
NM_005236.2:c.1763T>C , LRG_463t1:c.1763T>C
|
NP_005227.1:p.Val588Ala
|
|
XM_011522424.1:c.1901T>C
|
XP_011520726.1:p.Val634Ala
|
|
XM_011522425.1:c.1220T>C
|
XP_011520727.1:p.Val407Ala
|
|
XM_011522426.1:c.974T>C
|
XP_011520728.1:p.Val325Ala
|
|
XM_011522427.1:c.413T>C
|
XP_011520729.1:p.Val138Ala
|
|
XR_932805.1:n.1922T>C
|
|
|
XM_011522424.3:c.1901T>C
|
XP_011520726.1:p.Val634Ala
|
|
XM_017023043.2:c.974T>C
|
XP_016878532.1:p.Val325Ala
|
|
NM_005236.3:c.1763T>C
MANE Select
|
NP_005227.1:p.Val588Ala
|
|