ENST00000336079.8:c.1146T>G
MANE Select
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ENSP00000336725.3:p.Thr382=
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ENST00000336079.7:c.1146T>G
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ENSP00000336725.3:p.Thr382=
|
|
ENST00000360160.8:c.1146T>G
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ENSP00000353284.4:p.Thr382=
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ENST00000495478.1:n.261T>G
|
|
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NM_001122665.2:c.1146T>G
|
NP_001116137.1:p.Thr382=
|
|
NM_001302552.1:c.1137T>G
|
NP_001289481.1:p.Thr379=
|
|
NM_004660.4:c.1146T>G
|
NP_004651.2:p.Thr382=
|
|
XM_006724878.1:c.1146T>G
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XP_006724941.1:p.Thr382=
|
|
XM_011531471.1:c.1146T>G
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XP_011529773.1:p.Thr382=
|
|
NM_001122665.3:c.1146T>G
|
NP_001116137.1:p.Thr382=
|
|
NM_001302552.2:c.1137T>G
|
NP_001289481.1:p.Thr379=
|
|
NM_001324195.1:c.1146T>G
|
NP_001311124.1:p.Thr382=
|
|
NR_136716.1:n.1615T>G
|
|
|
NR_136717.1:n.1377T>G
|
|
|
NR_136718.1:n.1695T>G
|
|
|
NR_136719.1:n.1485T>G
|
|
|
NR_136720.1:n.1615T>G
|
|
|
NR_136721.1:n.1208T>G
|
|
|
NR_136722.1:n.1292T>G
|
|
|
NR_136723.1:n.1610T>G
|
|
|
NR_136724.1:n.1530T>G
|
|
|
XR_001756014.2:n.1250T>G
|
|
|
NM_004660.5:c.1146T>G
MANE Select
|
NP_004651.2:p.Thr382=
|
|
NM_001302552.3:c.1137T>G
|
NP_001289481.1:p.Thr379=
|
|
NM_001324195.2:c.1146T>G
|
NP_001311124.1:p.Thr382=
|
|
NR_136716.2:n.1533T>G
|
|
|
NR_136717.2:n.1295T>G
|
|
|
NR_136718.2:n.1613T>G
|
|
|
NR_136719.2:n.1403T>G
|
|
|
NR_136720.2:n.1533T>G
|
|
|
NR_136721.2:n.1198T>G
|
|
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