ENST00000302850.10:c.3894T=
MANE Select
|
ENSP00000303830.4:p.Phe1298=
|
|
ENST00000302850.9:c.3894T=
|
ENSP00000303830.4:p.Phe1298=
|
|
ENST00000341500.9:c.3858T=
|
ENSP00000342838.4:p.Phe1286=
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|
NM_000208.2:c.3894T=
|
NP_000199.2:p.Phe1298=
|
|
NM_000208.3:c.3894T=
|
NP_000199.2:p.Phe1298=
|
|
NM_001079817.1:c.3858T=
|
NP_001073285.1:p.Phe1286=
|
|
NM_001079817.2:c.3858T=
|
NP_001073285.1:p.Phe1286=
|
|
XM_011527988.1:c.3969T=
|
XP_011526290.1:p.Phe1323=
|
|
XM_011527989.1:c.3933T=
|
XP_011526291.1:p.Phe1311=
|
|
XM_011527988.2:c.3891T=
|
XP_011526290.2:p.Phe1297=
|
|
XM_011527989.3:c.3855T=
|
XP_011526291.2:p.Phe1285=
|
|
NM_000208.4:c.3894T=
MANE Select
|
NP_000199.2:p.Phe1298=
|
|
NM_001079817.3:c.3858T=
|
NP_001073285.1:p.Phe1286=
|
|