ENST00000682568.1:n.1626A>G
|
|
|
ENST00000682617.1:c.1686A>G
|
ENSP00000507912.1:p.Arg562=
|
|
ENST00000682826.1:c.*862A>G
|
ENSP00000507274.1:n.*862A>G
|
|
ENST00000682909.1:n.3588A>G
|
|
|
ENST00000683277.1:n.3193A>G
|
|
|
ENST00000683407.1:n.1556A>G
|
|
|
ENST00000683962.1:c.*1242A>G
|
ENSP00000506854.1:n.*1242A>G
|
|
ENST00000311895.8:c.1548A>G
MANE Select
|
ENSP00000310520.7:p.Arg516=
|
|
ENST00000311895.7:c.1548A>G
|
ENSP00000310520.7:p.Arg516=
|
|
ENST00000389138.7:n.825A>G
|
|
|
NM_005236.2:c.1548A>G , LRG_463t1:c.1548A>G
|
NP_005227.1:p.Arg516=
|
|
XM_011522424.1:c.1686A>G
|
XP_011520726.1:p.Arg562=
|
|
XM_011522425.1:c.1005A>G
|
XP_011520727.1:p.Arg335=
|
|
XM_011522426.1:c.759A>G
|
XP_011520728.1:p.Arg253=
|
|
XM_011522427.1:c.198A>G
|
XP_011520729.1:p.Arg66=
|
|
XR_932805.1:n.1707A>G
|
|
|
XM_011522424.3:c.1686A>G
|
XP_011520726.1:p.Arg562=
|
|
XM_017023043.2:c.759A>G
|
XP_016878532.1:p.Arg253=
|
|
NM_005236.3:c.1548A>G
MANE Select
|
NP_005227.1:p.Arg516=
|
|