ENST00000456935.7:c.1138T>C
MANE Select
|
ENSP00000395473.2:p.Tyr380His
|
|
ENST00000221363.8:c.1135T>C
|
ENSP00000221363.4:p.Tyr379His
|
|
ENST00000456935.6:c.1138T>C
|
ENSP00000395473.2:p.Tyr380His
|
|
ENST00000465830.1:n.302T>C
|
|
|
ENST00000466794.5:n.1037T>C
|
|
|
ENST00000495617.1:n.280+415T>C
|
|
|
NM_000528.3:c.1138T>C
|
NP_000519.2:p.Tyr380His
|
|
NM_001173498.1:c.1135T>C
|
NP_001166969.1:p.Tyr379His
|
|
XM_005259913.1:c.1141T>C
|
XP_005259970.1:p.Tyr381His
|
|
XM_011528017.1:c.37T>C
|
XP_011526319.1:p.Tyr13His
|
|
XM_005259913.2:c.1141T>C
|
XP_005259970.1:p.Tyr381His
|
|
XM_024451518.1:c.37T>C
|
XP_024307286.1:p.Tyr13His
|
|
NM_000528.4:c.1138T>C
MANE Select
|
NP_000519.2:p.Tyr380His
|
|
NM_001173498.2:c.1135T>C
|
NP_001166969.1:p.Tyr379His
|
|