ENST00000302850.10:c.3086T>G
MANE Select
|
ENSP00000303830.4:p.Leu1029Arg
|
|
ENST00000302850.9:c.3086T>G
|
ENSP00000303830.4:p.Leu1029Arg
|
|
ENST00000341500.9:c.3050T>G
|
ENSP00000342838.4:p.Leu1017Arg
|
|
NM_000208.2:c.3086T>G
|
NP_000199.2:p.Leu1029Arg
|
|
NM_000208.3:c.3086T>G
|
NP_000199.2:p.Leu1029Arg
|
|
NM_001079817.1:c.3050T>G
|
NP_001073285.1:p.Leu1017Arg
|
|
NM_001079817.2:c.3050T>G
|
NP_001073285.1:p.Leu1017Arg
|
|
XM_011527988.1:c.3161T>G
|
XP_011526290.1:p.Leu1054Arg
|
|
XM_011527989.1:c.3125T>G
|
XP_011526291.1:p.Leu1042Arg
|
|
XM_011527988.2:c.3083T>G
|
XP_011526290.2:p.Leu1028Arg
|
|
XM_011527989.3:c.3047T>G
|
XP_011526291.2:p.Leu1016Arg
|
|
NM_000208.4:c.3086T>G
MANE Select
|
NP_000199.2:p.Leu1029Arg
|
|
NM_001079817.3:c.3050T>G
|
NP_001073285.1:p.Leu1017Arg
|
|