ENST00000302850.10:c.3216C>A
MANE Select
|
ENSP00000303830.4:p.Leu1072=
|
|
ENST00000302850.9:c.3216C>A
|
ENSP00000303830.4:p.Leu1072=
|
|
ENST00000341500.9:c.3180C>A
|
ENSP00000342838.4:p.Leu1060=
|
|
ENST00000593970.1:n.62C>A
|
|
|
NM_000208.2:c.3216C>A
|
NP_000199.2:p.Leu1072=
|
|
NM_000208.3:c.3216C>A
|
NP_000199.2:p.Leu1072=
|
|
NM_001079817.1:c.3180C>A
|
NP_001073285.1:p.Leu1060=
|
|
NM_001079817.2:c.3180C>A
|
NP_001073285.1:p.Leu1060=
|
|
XM_011527988.1:c.3291C>A
|
XP_011526290.1:p.Leu1097=
|
|
XM_011527989.1:c.3255C>A
|
XP_011526291.1:p.Leu1085=
|
|
XM_011527988.2:c.3213C>A
|
XP_011526290.2:p.Leu1071=
|
|
XM_011527989.3:c.3177C>A
|
XP_011526291.2:p.Leu1059=
|
|
NM_000208.4:c.3216C>A
MANE Select
|
NP_000199.2:p.Leu1072=
|
|
NM_001079817.3:c.3180C>A
|
NP_001073285.1:p.Leu1060=
|
|