ENST00000261937.11:c.3970C>A
MANE Select
|
ENSP00000261937.6:p.Arg1324=
|
|
ENST00000261937.10:c.3970C>A
|
ENSP00000261937.6:p.Arg1324=
|
|
ENST00000502603.5:n.670C>A
|
|
|
NM_182925.4:c.3970C>A
|
NP_891555.2:p.Arg1324=
|
|
XM_011534477.1:c.4219C>A
|
XP_011532779.1:p.Arg1407=
|
|
XM_011534478.1:c.4201C>A
|
XP_011532780.1:p.Arg1401=
|
|
XM_011534479.1:c.*116C>A
|
XP_011532781.1:n.*116C>A
|
|
XM_011534482.1:c.3988C>A
|
XP_011532784.1:p.Arg1330=
|
|
XM_011534483.1:c.3910C>A
|
XP_011532785.1:p.Arg1304=
|
|
XM_011534484.1:c.3511C>A
|
XP_011532786.1:p.Arg1171=
|
|
XR_941095.1:n.4256C>A
|
|
|
XM_011534478.3:c.4201C>A
|
XP_011532780.1:p.Arg1401=
|
|
XM_011534484.2:c.3511C>A
|
XP_011532786.1:p.Arg1171=
|
|
XM_017009263.1:c.*116C>A
|
XP_016864752.1:n.*116C>A
|
|
XM_017009268.1:c.3892C>A
|
XP_016864757.1:p.Arg1298=
|
|
XR_001742050.2:n.4460C>A
|
|
|
NM_182925.5:c.3970C>A
MANE Select
|
NP_891555.2:p.Arg1324=
|
|