ENST00000262367.10:c.4484A>T
MANE Select
|
ENSP00000262367.5:p.Lys1495Met
|
|
ENST00000262367.9:c.4484A>T
|
ENSP00000262367.5:p.Lys1495Met
|
|
ENST00000382070.7:c.4370A>T
|
ENSP00000371502.3:p.Lys1457Met
|
|
ENST00000570939.2:c.3119A>T
|
ENSP00000461002.2:p.Lys1040Met
|
|
ENST00000571763.5:n.274A>T
|
|
|
ENST00000574740.1:n.305A>T
|
|
|
ENST00000576720.1:n.3307A>T
|
|
|
NM_001079846.1:c.4370A>T
|
NP_001073315.1:p.Lys1457Met
|
|
NM_004380.2:c.4484A>T
|
NP_004371.2:p.Lys1495Met
|
|
XM_005255124.3:c.4439A>T
|
XP_005255181.1:p.Lys1480Met
|
|
XM_005255125.3:c.4067A>T
|
XP_005255182.1:p.Lys1356Met
|
|
XM_006720848.2:c.4223A>T
|
XP_006720911.1:p.Lys1408Met
|
|
XM_011522380.1:c.4430A>T
|
XP_011520682.1:p.Lys1477Met
|
|
XM_011522381.1:c.3731A>T
|
XP_011520683.1:p.Lys1244Met
|
|
XM_005255124.4:c.4439A>T
|
XP_005255181.1:p.Lys1480Met
|
|
XM_005255125.4:c.4067A>T
|
XP_005255182.1:p.Lys1356Met
|
|
XM_006720848.3:c.4223A>T
|
XP_006720911.1:p.Lys1408Met
|
|
XM_011522381.2:c.3731A>T
|
XP_011520683.1:p.Lys1244Met
|
|
XM_017022944.1:c.4478A>T
|
XP_016878433.1:p.Lys1493Met
|
|
NM_004380.3:c.4484A>T
MANE Select
|
NP_004371.2:p.Lys1495Met
|
|