ENST00000261937.11:c.3960G>T
MANE Select
|
ENSP00000261937.6:p.Arg1320=
|
|
ENST00000261937.10:c.3960G>T
|
ENSP00000261937.6:p.Arg1320=
|
|
ENST00000502603.5:n.660G>T
|
|
|
NM_182925.4:c.3960G>T
|
NP_891555.2:p.Arg1320=
|
|
XM_011534477.1:c.4209G>T
|
XP_011532779.1:p.Arg1403=
|
|
XM_011534478.1:c.4191G>T
|
XP_011532780.1:p.Arg1397=
|
|
XM_011534479.1:c.*106G>T
|
XP_011532781.1:n.*106G>T
|
|
XM_011534482.1:c.3978G>T
|
XP_011532784.1:p.Arg1326=
|
|
XM_011534483.1:c.3900G>T
|
XP_011532785.1:p.Arg1300=
|
|
XM_011534484.1:c.3501G>T
|
XP_011532786.1:p.Arg1167=
|
|
XR_941095.1:n.4246G>T
|
|
|
XM_011534478.3:c.4191G>T
|
XP_011532780.1:p.Arg1397=
|
|
XM_011534484.2:c.3501G>T
|
XP_011532786.1:p.Arg1167=
|
|
XM_017009263.1:c.*106G>T
|
XP_016864752.1:n.*106G>T
|
|
XM_017009268.1:c.3882G>T
|
XP_016864757.1:p.Arg1294=
|
|
XR_001742050.2:n.4450G>T
|
|
|
NM_182925.5:c.3960G>T
MANE Select
|
NP_891555.2:p.Arg1320=
|
|