ENST00000339818.9:c.667C>G
MANE Select
|
ENSP00000344566.4:p.Leu223Val
|
|
ENST00000325223.7:c.664C>G
|
ENSP00000317302.7:p.Leu222Val
|
|
ENST00000339818.8:c.667C>G
|
ENSP00000344566.4:p.Leu223Val
|
|
ENST00000397956.7:c.1024C>G
|
ENSP00000381047.3:p.Leu342Val
|
|
ENST00000462742.1:n.4121C>G
|
|
|
ENST00000470196.5:n.243C>G
|
|
|
ENST00000496321.5:n.780C>G
|
|
|
NM_001271440.1:c.664C>G
|
NP_001258369.1:p.Leu222Val
|
|
NM_001271441.1:c.1024C>G
|
NP_001258370.1:p.Leu342Val
|
|
NM_001271442.1:c.541C>G
|
NP_001258371.1:p.Leu181Val
|
|
NM_004928.2:c.667C>G
|
NP_004919.1:p.Leu223Val
|
|
XM_006724051.2:c.742C>G
|
XP_006724114.1:p.Leu248Val
|
|
XM_006724052.2:c.739C>G
|
XP_006724115.1:p.Leu247Val
|
|
XM_006724053.2:c.343C>G
|
XP_006724116.1:p.Leu115Val
|
|
XR_937571.1:n.1227C>G
|
|
|
XM_006724051.3:c.742C>G
|
XP_006724114.1:p.Leu248Val
|
|
XM_006724053.3:c.343C>G
|
XP_006724116.1:p.Leu115Val
|
|
XM_017028470.1:c.868C>G
|
XP_016883959.1:p.Leu290Val
|
|
XM_017028471.1:c.616C>G
|
XP_016883960.1:p.Leu206Val
|
|
XM_017028472.1:c.340C>G
|
XP_016883961.1:p.Leu114Val
|
|
XR_937571.2:n.1234C>G
|
|
|
NM_004928.3:c.667C>G
MANE Select
|
NP_004919.1:p.Leu223Val
|
|
NM_001271440.2:c.664C>G
|
NP_001258369.1:p.Leu222Val
|
|
NM_001271441.2:c.1024C>G
|
NP_001258370.1:p.Leu342Val
|
|