ENST00000449082.3:c.4924T>G
MANE Select
|
ENSP00000390600.2:p.Phe1642Val
|
|
ENST00000643924.1:c.4921T>G
|
ENSP00000495595.1:p.Phe1641Val
|
|
ENST00000655275.1:c.4948T>G
|
ENSP00000499510.1:p.Phe1650Val
|
|
ENST00000449082.2:c.4924T>G
|
ENSP00000390600.2:p.Phe1642Val
|
|
NM_001293306.2:c.4921T>G
|
NP_001280235.2:p.Phe1641Val
|
|
NM_001293307.2:c.4630T>G
|
NP_001280236.2:p.Phe1544Val
|
|
NM_006514.3:c.4924T>G
|
NP_006505.3:p.Phe1642Val
|
|
XM_005265371.2:c.4933T>G
|
XP_005265428.1:p.Phe1645Val
|
|
XM_011533993.1:c.4930T>G
|
XP_011532295.1:p.Phe1644Val
|
|
XM_011533994.1:c.4639T>G
|
XP_011532296.1:p.Phe1547Val
|
|
XM_005265371.3:c.4933T>G
|
XP_005265428.1:p.Phe1645Val
|
|
XM_011533993.2:c.4930T>G
|
XP_011532295.1:p.Phe1644Val
|
|
XM_011533994.2:c.4639T>G
|
XP_011532296.1:p.Phe1547Val
|
|
NM_006514.4:c.4924T>G
MANE Select
|
NP_006505.4:p.Phe1642Val
|
|