ENST00000302850.10:c.2688G>T
MANE Select
|
ENSP00000303830.4:p.Leu896=
|
|
ENST00000302850.9:c.2688G>T
|
ENSP00000303830.4:p.Leu896=
|
|
ENST00000341500.9:c.2652G>T
|
ENSP00000342838.4:p.Leu884=
|
|
NM_000208.2:c.2688G>T
|
NP_000199.2:p.Leu896=
|
|
NM_000208.3:c.2688G>T
|
NP_000199.2:p.Leu896=
|
|
NM_001079817.1:c.2652G>T
|
NP_001073285.1:p.Leu884=
|
|
NM_001079817.2:c.2652G>T
|
NP_001073285.1:p.Leu884=
|
|
XM_011527988.1:c.2766G>T
|
XP_011526290.1:p.Leu922=
|
|
XM_011527989.1:c.2730G>T
|
XP_011526291.1:p.Leu910=
|
|
XM_011527988.2:c.2688G>T
|
XP_011526290.2:p.Leu896=
|
|
XM_011527989.3:c.2652G>T
|
XP_011526291.2:p.Leu884=
|
|
NM_000208.4:c.2688G>T
MANE Select
|
NP_000199.2:p.Leu896=
|
|
NM_001079817.3:c.2652G>T
|
NP_001073285.1:p.Leu884=
|
|