ENST00000302850.10:c.4126T>C
MANE Select
|
ENSP00000303830.4:p.Leu1376=
|
|
ENST00000302850.9:c.4126T>C
|
ENSP00000303830.4:p.Leu1376=
|
|
ENST00000341500.9:c.4090T>C
|
ENSP00000342838.4:p.Leu1364=
|
|
NM_000208.2:c.4126T>C
|
NP_000199.2:p.Leu1376=
|
|
NM_000208.3:c.4126T>C
|
NP_000199.2:p.Leu1376=
|
|
NM_001079817.1:c.4090T>C
|
NP_001073285.1:p.Leu1364=
|
|
NM_001079817.2:c.4090T>C
|
NP_001073285.1:p.Leu1364=
|
|
XM_011527988.1:c.4201T>C
|
XP_011526290.1:p.Leu1401=
|
|
XM_011527989.1:c.4165T>C
|
XP_011526291.1:p.Leu1389=
|
|
XM_011527988.2:c.4123T>C
|
XP_011526290.2:p.Leu1375=
|
|
XM_011527989.3:c.4087T>C
|
XP_011526291.2:p.Leu1363=
|
|
NM_000208.4:c.4126T>C
MANE Select
|
NP_000199.2:p.Leu1376=
|
|
NM_001079817.3:c.4090T>C
|
NP_001073285.1:p.Leu1364=
|
|