ENST00000336079.8:c.1177G>T
MANE Select
|
ENSP00000336725.3:p.Asp393Tyr
|
|
ENST00000336079.7:c.1177G>T
|
ENSP00000336725.3:p.Asp393Tyr
|
|
ENST00000360160.8:c.1177G>T
|
ENSP00000353284.4:p.Asp393Tyr
|
|
ENST00000495478.1:n.292G>T
|
|
|
NM_001122665.2:c.1177G>T
|
NP_001116137.1:p.Asp393Tyr
|
|
NM_001302552.1:c.1168G>T
|
NP_001289481.1:p.Asp390Tyr
|
|
NM_004660.4:c.1177G>T
|
NP_004651.2:p.Asp393Tyr
|
|
XM_006724878.1:c.1177G>T
|
XP_006724941.1:p.Asp393Tyr
|
|
XM_011531471.1:c.1177G>T
|
XP_011529773.1:p.Asp393Tyr
|
|
NM_001122665.3:c.1177G>T
|
NP_001116137.1:p.Asp393Tyr
|
|
NM_001302552.2:c.1168G>T
|
NP_001289481.1:p.Asp390Tyr
|
|
NM_001324195.1:c.1177G>T
|
NP_001311124.1:p.Asp393Tyr
|
|
NR_136716.1:n.1646G>T
|
|
|
NR_136717.1:n.1408G>T
|
|
|
NR_136718.1:n.1726G>T
|
|
|
NR_136719.1:n.1516G>T
|
|
|
NR_136720.1:n.1646G>T
|
|
|
NR_136721.1:n.1239G>T
|
|
|
NR_136722.1:n.1323G>T
|
|
|
NR_136723.1:n.1641G>T
|
|
|
NR_136724.1:n.1561G>T
|
|
|
XR_001756014.2:n.1281G>T
|
|
|
NM_004660.5:c.1177G>T
MANE Select
|
NP_004651.2:p.Asp393Tyr
|
|
NM_001302552.3:c.1168G>T
|
NP_001289481.1:p.Asp390Tyr
|
|
NM_001324195.2:c.1177G>T
|
NP_001311124.1:p.Asp393Tyr
|
|
NR_136716.2:n.1564G>T
|
|
|
NR_136717.2:n.1326G>T
|
|
|
NR_136718.2:n.1644G>T
|
|
|
NR_136719.2:n.1434G>T
|
|
|
NR_136720.2:n.1564G>T
|
|
|
NR_136721.2:n.1229G>T
|
|
|