ENST00000261937.11:c.3955C>A
MANE Select
|
ENSP00000261937.6:p.Arg1319=
|
|
ENST00000261937.10:c.3955C>A
|
ENSP00000261937.6:p.Arg1319=
|
|
ENST00000502603.5:n.655C>A
|
|
|
NM_182925.4:c.3955C>A
|
NP_891555.2:p.Arg1319=
|
|
XM_011534477.1:c.4204C>A
|
XP_011532779.1:p.Arg1402=
|
|
XM_011534478.1:c.4186C>A
|
XP_011532780.1:p.Arg1396=
|
|
XM_011534479.1:c.*101C>A
|
XP_011532781.1:n.*101C>A
|
|
XM_011534482.1:c.3973C>A
|
XP_011532784.1:p.Arg1325=
|
|
XM_011534483.1:c.3895C>A
|
XP_011532785.1:p.Arg1299=
|
|
XM_011534484.1:c.3496C>A
|
XP_011532786.1:p.Arg1166=
|
|
XR_941095.1:n.4241C>A
|
|
|
XM_011534478.3:c.4186C>A
|
XP_011532780.1:p.Arg1396=
|
|
XM_011534484.2:c.3496C>A
|
XP_011532786.1:p.Arg1166=
|
|
XM_017009263.1:c.*101C>A
|
XP_016864752.1:n.*101C>A
|
|
XM_017009268.1:c.3877C>A
|
XP_016864757.1:p.Arg1293=
|
|
XR_001742050.2:n.4445C>A
|
|
|
NM_182925.5:c.3955C>A
MANE Select
|
NP_891555.2:p.Arg1319=
|
|