ENST00000237596.7:c.843G>A
MANE Select
|
ENSP00000237596.2:p.Lys281=
|
|
ENST00000237596.6:c.843G>A
|
ENSP00000237596.2:p.Lys281=
|
|
ENST00000506367.1:n.290G>A
|
|
|
ENST00000506727.1:n.429G>A
|
|
|
NM_000297.3:c.843G>A
|
NP_000288.1:p.Lys281=
|
|
XM_011532028.1:c.843G>A
|
XP_011530330.1:p.Lys281=
|
|
XM_011532029.1:c.123G>A
|
XP_011530331.1:p.Lys41=
|
|
XR_244632.2:n.938G>A
|
|
|
NR_156488.1:n.930G>A
|
|
|
XM_011532028.2:c.843G>A
|
XP_011530330.1:p.Lys281=
|
|
XM_011532030.2:c.-125G>A
|
XP_011530332.1:n.-125G>A
|
|
NM_000297.4:c.843G>A
MANE Select
|
NP_000288.1:p.Lys281=
|
|
NR_156488.2:n.942G>A
|
|
|