ENST00000302850.10:c.3987G>A
MANE Select
|
ENSP00000303830.4:p.Leu1329=
|
|
ENST00000302850.9:c.3987G>A
|
ENSP00000303830.4:p.Leu1329=
|
|
ENST00000341500.9:c.3951G>A
|
ENSP00000342838.4:p.Leu1317=
|
|
NM_000208.2:c.3987G>A
|
NP_000199.2:p.Leu1329=
|
|
NM_000208.3:c.3987G>A
|
NP_000199.2:p.Leu1329=
|
|
NM_001079817.1:c.3951G>A
|
NP_001073285.1:p.Leu1317=
|
|
NM_001079817.2:c.3951G>A
|
NP_001073285.1:p.Leu1317=
|
|
XM_011527988.1:c.4062G>A
|
XP_011526290.1:p.Leu1354=
|
|
XM_011527989.1:c.4026G>A
|
XP_011526291.1:p.Leu1342=
|
|
XM_011527988.2:c.3984G>A
|
XP_011526290.2:p.Leu1328=
|
|
XM_011527989.3:c.3948G>A
|
XP_011526291.2:p.Leu1316=
|
|
NM_000208.4:c.3987G>A
MANE Select
|
NP_000199.2:p.Leu1329=
|
|
NM_001079817.3:c.3951G>A
|
NP_001073285.1:p.Leu1317=
|
|