ENST00000301244.12:c.488A>G
MANE Select
|
ENSP00000301244.5:p.Tyr163Cys
|
|
ENST00000301244.11:c.488A>G
|
ENSP00000301244.5:p.Tyr163Cys
|
|
ENST00000454580.7:c.317A>G
|
ENSP00000389788.2:p.Tyr106Cys
|
|
ENST00000585357.1:n.1810A>G
|
|
|
ENST00000587090.5:c.338A>G
|
ENSP00000466407.1:p.Tyr113Cys
|
|
ENST00000587334.1:c.29A>G
|
|
|
ENST00000587516.5:c.428A>G
|
ENSP00000465721.1:p.Tyr143Cys
|
|
ENST00000587519.4:c.138A>G
|
|
|
ENST00000589749.1:n.408A>G
|
|
|
ENST00000590738.1:c.151A>G
|
|
|
ENST00000591889.2:c.121A>G
|
|
|
NM_001166103.1:c.317A>G
|
NP_001159575.1:p.Tyr106Cys
|
|
NM_021102.3:c.488A>G
|
NP_066925.1:p.Tyr163Cys
|
|
NM_021102.4:c.488A>G
MANE Select
|
NP_066925.1:p.Tyr163Cys
|
|
NM_001166103.2:c.317A>G
|
NP_001159575.1:p.Tyr106Cys
|
|