ENST00000302850.10:c.3892T>G
MANE Select
|
ENSP00000303830.4:p.Phe1298Val
|
|
ENST00000302850.9:c.3892T>G
|
ENSP00000303830.4:p.Phe1298Val
|
|
ENST00000341500.9:c.3856T>G
|
ENSP00000342838.4:p.Phe1286Val
|
|
NM_000208.2:c.3892T>G
|
NP_000199.2:p.Phe1298Val
|
|
NM_000208.3:c.3892T>G
|
NP_000199.2:p.Phe1298Val
|
|
NM_001079817.1:c.3856T>G
|
NP_001073285.1:p.Phe1286Val
|
|
NM_001079817.2:c.3856T>G
|
NP_001073285.1:p.Phe1286Val
|
|
XM_011527988.1:c.3967T>G
|
XP_011526290.1:p.Phe1323Val
|
|
XM_011527989.1:c.3931T>G
|
XP_011526291.1:p.Phe1311Val
|
|
XM_011527988.2:c.3889T>G
|
XP_011526290.2:p.Phe1297Val
|
|
XM_011527989.3:c.3853T>G
|
XP_011526291.2:p.Phe1285Val
|
|
NM_000208.4:c.3892T>G
MANE Select
|
NP_000199.2:p.Phe1298Val
|
|
NM_001079817.3:c.3856T>G
|
NP_001073285.1:p.Phe1286Val
|
|