ENST00000302850.10:c.2772A>G
MANE Select
|
ENSP00000303830.4:p.Arg924=
|
|
ENST00000302850.9:c.2772A>G
|
ENSP00000303830.4:p.Arg924=
|
|
ENST00000341500.9:c.2736A>G
|
ENSP00000342838.4:p.Arg912=
|
|
NM_000208.2:c.2772A>G
|
NP_000199.2:p.Arg924=
|
|
NM_000208.3:c.2772A>G
|
NP_000199.2:p.Arg924=
|
|
NM_001079817.1:c.2736A>G
|
NP_001073285.1:p.Arg912=
|
|
NM_001079817.2:c.2736A>G
|
NP_001073285.1:p.Arg912=
|
|
XM_011527988.1:c.2850A>G
|
XP_011526290.1:p.Arg950=
|
|
XM_011527989.1:c.2814A>G
|
XP_011526291.1:p.Arg938=
|
|
XM_011527988.2:c.2772A>G
|
XP_011526290.2:p.Arg924=
|
|
XM_011527989.3:c.2736A>G
|
XP_011526291.2:p.Arg912=
|
|
NM_000208.4:c.2772A>G
MANE Select
|
NP_000199.2:p.Arg924=
|
|
NM_001079817.3:c.2736A>G
|
NP_001073285.1:p.Arg912=
|
|