ENST00000290866.10:c.3673A>T
MANE Select
|
ENSP00000290866.4:p.Asn1225Tyr
|
|
ENST00000290863.10:c.1951A>T
|
ENSP00000290863.6:p.Asn651Tyr
|
|
ENST00000290866.9:c.3673A>T
|
ENSP00000290866.4:p.Asn1225Tyr
|
|
ENST00000413513.7:c.1828A>T
|
ENSP00000392247.3:p.Asn610Tyr
|
|
ENST00000428043.5:c.3673A>T
|
ENSP00000397593.2:p.Asn1225Tyr
|
|
ENST00000577418.5:n.683A>T
|
|
|
ENST00000577647.2:c.1951A>T
|
ENSP00000464149.1:p.Asn651Tyr
|
|
ENST00000578839.5:c.*1428A>T
|
ENSP00000462110.2:n.*1428A>T
|
|
ENST00000579314.5:c.*1402A>T
|
ENSP00000462599.1:n.*1402A>T
|
|
ENST00000579409.1:c.360A>T
|
|
|
ENST00000582244.1:n.547A>T
|
|
|
NM_000789.3:c.3673A>T
|
NP_000780.1:p.Asn1225Tyr
|
|
NM_001178057.1:c.1828A>T
|
NP_001171528.1:p.Asn610Tyr
|
|
NM_152830.2:c.1951A>T
|
NP_690043.1:p.Asn651Tyr
|
|
XM_005257110.1:c.3124A>T
|
XP_005257167.1:p.Asn1042Tyr
|
|
XM_006721737.2:c.2011A>T
|
XP_006721800.2:p.Asn671Tyr
|
|
XM_006721737.3:c.2011A>T
|
XP_006721800.2:p.Asn671Tyr
|
|
NM_000789.4:c.3673A>T
MANE Select
|
NP_000780.1:p.Asn1225Tyr
|
|
NM_001178057.2:c.1828A>T
|
NP_001171528.1:p.Asn610Tyr
|
|
NM_152830.3:c.1951A>T
|
NP_690043.1:p.Asn651Tyr
|
|
NM_001382700.1:c.3106A>T
|
NP_001369629.1:p.Asn1036Tyr
|
|
NM_001382701.1:c.2821A>T
|
NP_001369630.1:p.Asn941Tyr
|
|
NM_001382702.1:c.1288A>T
|
NP_001369631.1:p.Asn430Tyr
|
|
NR_168483.1:n.2051A>T
|
|
|