ENST00000272602.7:c.709A>T
MANE Select
|
ENSP00000272602.2:p.Asn237Tyr
|
|
ENST00000272602.6:c.709A>T
|
ENSP00000272602.2:p.Asn237Tyr
|
|
ENST00000393504.5:c.709A>T
|
ENSP00000377140.1:p.Asn237Tyr
|
|
ENST00000409937.1:c.721A>T
|
ENSP00000386761.1:p.Asn241Tyr
|
|
ENST00000436404.6:c.655A>T
|
ENSP00000410070.2:p.Asn219Tyr
|
|
NM_001079878.1:c.655A>T
|
NP_001073347.1:p.Asn219Tyr
|
|
NM_001298.2:c.709A>T
|
NP_001289.1:p.Asn237Tyr
|
|
XM_006712243.2:c.820A>T
|
XP_006712306.1:p.Asn274Tyr
|
|
XM_011510554.1:c.874A>T
|
XP_011508856.1:p.Asn292Tyr
|
|
XM_011510554.2:c.874A>T
|
XP_011508856.1:p.Asn292Tyr
|
|
NM_001079878.2:c.655A>T
|
NP_001073347.1:p.Asn219Tyr
|
|
NM_001298.3:c.709A>T
MANE Select
|
NP_001289.1:p.Asn237Tyr
|
|