ENST00000262367.10:c.4410C>A
MANE Select
|
ENSP00000262367.5:p.His1470Gln
|
|
ENST00000262367.9:c.4410C>A
|
ENSP00000262367.5:p.His1470Gln
|
|
ENST00000382070.7:c.4296C>A
|
ENSP00000371502.3:p.His1432Gln
|
|
ENST00000570939.2:c.3045C>A
|
ENSP00000461002.2:p.His1015Gln
|
|
ENST00000571763.5:n.200C>A
|
|
|
ENST00000574740.1:n.231C>A
|
|
|
ENST00000576720.1:n.3233C>A
|
|
|
NM_001079846.1:c.4296C>A
|
NP_001073315.1:p.His1432Gln
|
|
NM_004380.2:c.4410C>A
|
NP_004371.2:p.His1470Gln
|
|
XM_005255124.3:c.4365C>A
|
XP_005255181.1:p.His1455Gln
|
|
XM_005255125.3:c.3993C>A
|
XP_005255182.1:p.His1331Gln
|
|
XM_006720848.2:c.4149C>A
|
XP_006720911.1:p.His1383Gln
|
|
XM_011522380.1:c.4356C>A
|
XP_011520682.1:p.His1452Gln
|
|
XM_011522381.1:c.3657C>A
|
XP_011520683.1:p.His1219Gln
|
|
XM_005255124.4:c.4365C>A
|
XP_005255181.1:p.His1455Gln
|
|
XM_005255125.4:c.3993C>A
|
XP_005255182.1:p.His1331Gln
|
|
XM_006720848.3:c.4149C>A
|
XP_006720911.1:p.His1383Gln
|
|
XM_011522381.2:c.3657C>A
|
XP_011520683.1:p.His1219Gln
|
|
XM_017022944.1:c.4404C>A
|
XP_016878433.1:p.His1468Gln
|
|
NM_004380.3:c.4410C>A
MANE Select
|
NP_004371.2:p.His1470Gln
|
|