ENST00000261937.11:c.4015G=
MANE Select
|
ENSP00000261937.6:p.Glu1339=
|
|
ENST00000261937.10:c.4015G=
|
ENSP00000261937.6:p.Glu1339=
|
|
ENST00000502603.5:n.715G=
|
|
|
NM_182925.4:c.4015G=
|
NP_891555.2:p.Glu1339=
|
|
XM_011534477.1:c.4264G=
|
XP_011532779.1:p.Glu1422=
|
|
XM_011534478.1:c.4246G=
|
XP_011532780.1:p.Glu1416=
|
|
XM_011534482.1:c.4033G=
|
XP_011532784.1:p.Glu1345=
|
|
XM_011534483.1:c.3955G=
|
XP_011532785.1:p.Glu1319=
|
|
XM_011534484.1:c.3556G=
|
XP_011532786.1:p.Glu1186=
|
|
XR_941095.1:n.4301G=
|
|
|
XM_011534478.3:c.4246G=
|
XP_011532780.1:p.Glu1416=
|
|
XM_011534484.2:c.3556G=
|
XP_011532786.1:p.Glu1186=
|
|
XM_017009263.1:c.*161G=
|
XP_016864752.1:n.*161G=
|
|
XM_017009268.1:c.3937G=
|
XP_016864757.1:p.Glu1313=
|
|
XR_001742050.2:n.4505G=
|
|
|
NM_182925.5:c.4015G=
MANE Select
|
NP_891555.2:p.Glu1339=
|
|