ENST00000682568.1:n.1872G>C
|
|
|
ENST00000682617.1:c.1932G>C
|
ENSP00000507912.1:p.Arg644Ser
|
|
ENST00000682826.1:c.*1108G>C
|
ENSP00000507274.1:n.*1108G>C
|
|
ENST00000682909.1:n.3834G>C
|
|
|
ENST00000683277.1:n.3439G>C
|
|
|
ENST00000683407.1:n.1802G>C
|
|
|
ENST00000683962.1:c.*1488G>C
|
ENSP00000506854.1:n.*1488G>C
|
|
ENST00000311895.8:c.1794G>C
MANE Select
|
ENSP00000310520.7:p.Arg598Ser
|
|
ENST00000311895.7:c.1794G>C
|
ENSP00000310520.7:p.Arg598Ser
|
|
ENST00000389138.7:n.1071G>C
|
|
|
NM_005236.2:c.1794G>C , LRG_463t1:c.1794G>C
|
NP_005227.1:p.Arg598Ser
|
|
XM_011522424.1:c.1932G>C
|
XP_011520726.1:p.Arg644Ser
|
|
XM_011522425.1:c.1251G>C
|
XP_011520727.1:p.Arg417Ser
|
|
XM_011522426.1:c.1005G>C
|
XP_011520728.1:p.Arg335Ser
|
|
XM_011522427.1:c.444G>C
|
XP_011520729.1:p.Arg148Ser
|
|
XR_932805.1:n.1953G>C
|
|
|
XM_011522424.3:c.1932G>C
|
XP_011520726.1:p.Arg644Ser
|
|
XM_017023043.2:c.1005G>C
|
XP_016878532.1:p.Arg335Ser
|
|
NM_005236.3:c.1794G>C
MANE Select
|
NP_005227.1:p.Arg598Ser
|
|