ENST00000682114.1:c.545A>G
|
ENSP00000507245.1:p.Tyr182Cys
|
|
ENST00000682478.1:n.735A>G
|
|
|
ENST00000683576.1:n.735A>G
|
|
|
ENST00000683627.1:c.545A>G
|
ENSP00000507533.1:p.Tyr182Cys
|
|
ENST00000684082.1:c.502A>G
|
ENSP00000508266.1:n.502A>G
|
|
ENST00000684633.1:n.517A>G
|
|
|
ENST00000684678.1:c.541A>G
|
ENSP00000507059.1:n.541A>G
|
|
ENST00000369842.9:c.545A>G
MANE Select
|
ENSP00000358857.4:p.Tyr182Cys
|
|
ENST00000369835.3:c.440A>G
|
ENSP00000358850.3:p.Tyr147Cys
|
|
ENST00000369842.8:c.545A>G
|
ENSP00000358857.4:p.Tyr182Cys
|
|
ENST00000428228.5:c.*450A>G
|
ENSP00000401081.1:n.*450A>G
|
|
ENST00000471965.1:n.334A>G
|
|
|
ENST00000486738.5:n.982A>G
|
|
|
ENST00000492448.1:n.528A>G
|
|
|
NM_000117.2:c.545A>G , LRG_745t1:c.545A>G
|
NP_000108.1:p.Tyr182Cys
|
|
XM_024452349.1:c.551A>G
|
XP_024308117.1:p.Tyr184Cys
|
|
NM_000117.3:c.545A>G
MANE Select
|
NP_000108.1:p.Tyr182Cys
|
|