ENST00000252288.8:c.502T>C
MANE Select
|
ENSP00000252288.1:p.Tyr168His
|
|
ENST00000447102.8:c.502T>C
|
ENSP00000403536.2:p.Tyr168His
|
|
ENST00000591788.3:c.185T>C
|
|
|
ENST00000640164.1:n.335T>C
|
|
|
ENST00000640762.1:c.433T>C
|
ENSP00000492031.1:p.Tyr145His
|
|
ENST00000252288.6:c.502T>C
|
ENSP00000252288.1:p.Tyr168His
|
|
ENST00000447102.7:c.502T>C
|
ENSP00000403536.2:p.Tyr168His
|
|
ENST00000591788.2:c.187T>C
|
ENSP00000466341.2:p.Tyr63His
|
|
NM_000156.5:c.502T>C
|
NP_000147.1:p.Tyr168His
|
|
NM_138924.2:c.502T>C
|
NP_620279.1:p.Tyr168His
|
|
NM_000156.6:c.502T>C
MANE Select
|
NP_000147.1:p.Tyr168His
|
|
NM_138924.3:c.502T>C
|
NP_620279.1:p.Tyr168His
|
|