ENST00000302850.10:c.2284A>C
MANE Select
|
ENSP00000303830.4:p.Arg762=
|
|
ENST00000302850.9:c.2284A>C
|
ENSP00000303830.4:p.Arg762=
|
|
ENST00000341500.9:c.2248A>C
|
ENSP00000342838.4:p.Arg750=
|
|
NM_000208.2:c.2284A>C
|
NP_000199.2:p.Arg762=
|
|
NM_000208.3:c.2284A>C
|
NP_000199.2:p.Arg762=
|
|
NM_001079817.1:c.2248A>C
|
NP_001073285.1:p.Arg750=
|
|
NM_001079817.2:c.2248A>C
|
NP_001073285.1:p.Arg750=
|
|
XM_011527988.1:c.2362A>C
|
XP_011526290.1:p.Arg788=
|
|
XM_011527989.1:c.2326A>C
|
XP_011526291.1:p.Arg776=
|
|
XM_011527988.2:c.2284A>C
|
XP_011526290.2:p.Arg762=
|
|
XM_011527989.3:c.2248A>C
|
XP_011526291.2:p.Arg750=
|
|
NM_000208.4:c.2284A>C
MANE Select
|
NP_000199.2:p.Arg762=
|
|
NM_001079817.3:c.2248A>C
|
NP_001073285.1:p.Arg750=
|
|