ENST00000262367.10:c.4050T>A
MANE Select
|
ENSP00000262367.5:p.Asn1350Lys
|
|
ENST00000262367.9:c.4050T>A
|
ENSP00000262367.5:p.Asn1350Lys
|
|
ENST00000382070.7:c.3936T>A
|
ENSP00000371502.3:p.Asn1312Lys
|
|
ENST00000570939.2:c.2685T>A
|
ENSP00000461002.2:p.Asn895Lys
|
|
ENST00000572569.1:n.514T>A
|
|
|
ENST00000573517.6:c.356T>A
|
|
|
ENST00000574740.1:n.132T>A
|
|
|
ENST00000576720.1:n.2987T>A
|
|
|
NM_001079846.1:c.3936T>A
|
NP_001073315.1:p.Asn1312Lys
|
|
NM_004380.2:c.4050T>A
|
NP_004371.2:p.Asn1350Lys
|
|
XM_005255124.3:c.4005T>A
|
XP_005255181.1:p.Asn1335Lys
|
|
XM_005255125.3:c.3633T>A
|
XP_005255182.1:p.Asn1211Lys
|
|
XM_006720848.2:c.4050T>A
|
XP_006720911.1:p.Asn1350Lys
|
|
XM_011522380.1:c.3996T>A
|
XP_011520682.1:p.Asn1332Lys
|
|
XM_011522381.1:c.3297T>A
|
XP_011520683.1:p.Asn1099Lys
|
|
XM_005255124.4:c.4005T>A
|
XP_005255181.1:p.Asn1335Lys
|
|
XM_005255125.4:c.3633T>A
|
XP_005255182.1:p.Asn1211Lys
|
|
XM_006720848.3:c.4050T>A
|
XP_006720911.1:p.Asn1350Lys
|
|
XM_011522381.2:c.3297T>A
|
XP_011520683.1:p.Asn1099Lys
|
|
XM_017022944.1:c.4044T>A
|
XP_016878433.1:p.Asn1348Lys
|
|
NM_004380.3:c.4050T>A
MANE Select
|
NP_004371.2:p.Asn1350Lys
|
|