ENST00000302850.10:c.3910T>G
MANE Select
|
ENSP00000303830.4:p.Phe1304Val
|
|
ENST00000302850.9:c.3910T>G
|
ENSP00000303830.4:p.Phe1304Val
|
|
ENST00000341500.9:c.3874T>G
|
ENSP00000342838.4:p.Phe1292Val
|
|
NM_000208.2:c.3910T>G
|
NP_000199.2:p.Phe1304Val
|
|
NM_000208.3:c.3910T>G
|
NP_000199.2:p.Phe1304Val
|
|
NM_001079817.1:c.3874T>G
|
NP_001073285.1:p.Phe1292Val
|
|
NM_001079817.2:c.3874T>G
|
NP_001073285.1:p.Phe1292Val
|
|
XM_011527988.1:c.3985T>G
|
XP_011526290.1:p.Phe1329Val
|
|
XM_011527989.1:c.3949T>G
|
XP_011526291.1:p.Phe1317Val
|
|
XM_011527988.2:c.3907T>G
|
XP_011526290.2:p.Phe1303Val
|
|
XM_011527989.3:c.3871T>G
|
XP_011526291.2:p.Phe1291Val
|
|
NM_000208.4:c.3910T>G
MANE Select
|
NP_000199.2:p.Phe1304Val
|
|
NM_001079817.3:c.3874T>G
|
NP_001073285.1:p.Phe1292Val
|
|