ENST00000455688.2:c.379T>A
|
ENSP00000407204.2:p.Tyr127Asn
|
|
ENST00000477869.6:c.268T>A
|
ENSP00000496725.1:p.Tyr90Asn
|
|
ENST00000493869.2:c.305-591T>A
|
ENSP00000495713.1:n.305-591T>A
|
|
ENST00000650242.1:c.595T>A
MANE Select
|
ENSP00000497236.1:p.Tyr199Asn
|
|
ENST00000330807.9:c.595T>A
|
ENSP00000332369.5:p.Tyr199Asn
|
|
ENST00000335854.8:c.484T>A
|
ENSP00000337131.4:p.Tyr162Asn
|
|
ENST00000396198.7:c.556T>A
|
ENSP00000379501.3:p.Tyr186Asn
|
|
ENST00000455688.1:c.450T>A
|
|
|
ENST00000463868.5:n.356-591T>A
|
|
|
ENST00000477869.5:n.339T>A
|
|
|
ENST00000493869.1:n.535T>A
|
|
|
NM_000032.4:c.595T>A
|
NP_000023.2:p.Tyr199Asn
|
|
NM_001037967.3:c.484T>A
|
NP_001033056.1:p.Tyr162Asn
|
|
NM_001037968.3:c.556T>A
|
NP_001033057.1:p.Tyr186Asn
|
|
XM_005261995.2:c.667T>A
|
XP_005262052.1:p.Tyr223Asn
|
|
XM_011530771.1:c.-223-591T>A
|
XP_011529073.1:n.-223-591T>A
|
|
NM_000032.5:c.595T>A
MANE Select
|
NP_000023.2:p.Tyr199Asn
|
|
NM_001037967.4:c.484T>A
|
NP_001033056.1:p.Tyr162Asn
|
|
NM_001037968.4:c.556T>A
|
NP_001033057.1:p.Tyr186Asn
|
|