ENST00000370086.8:c.364A>T
MANE Select
|
ENSP00000359103.3:p.Asn122Tyr
|
|
ENST00000320857.7:c.364A>T
|
ENSP00000317331.3:p.Asn122Tyr
|
|
ENST00000370085.3:c.289A>T
|
ENSP00000359102.3:p.Asn97Tyr
|
|
ENST00000370086.7:c.364A>T
|
ENSP00000359103.3:p.Asn122Tyr
|
|
ENST00000370087.5:c.364A>T
|
ENSP00000359104.1:p.Asn122Tyr
|
|
ENST00000447375.1:n.204A>T
|
|
|
ENST00000460616.5:n.2072A>T
|
|
|
ENST00000471880.5:n.567A>T
|
|
|
ENST00000482902.5:n.2191A>T
|
|
|
ENST00000485612.5:n.479A>T
|
|
|
ENST00000486204.5:n.436A>T
|
|
|
NM_001204526.1:c.397A>T
|
NP_001191455.1:p.Asn133Tyr
|
|
NM_001204527.1:c.388A>T
|
NP_001191456.1:p.Asn130Tyr
|
|
NM_006280.2:c.364A>T
|
NP_006271.1:p.Asn122Tyr
|
|
NR_037927.1:n.709A>T
|
|
|
XM_011531186.1:c.364A>T
|
XP_011529488.1:p.Asn122Tyr
|
|
XM_011531187.1:c.364A>T
|
XP_011529489.1:p.Asn122Tyr
|
|
XM_017029756.1:c.175A>T
|
XP_016885245.1:p.Asn59Tyr
|
|
XM_017029757.1:c.175A>T
|
XP_016885246.1:p.Asn59Tyr
|
|
XM_024452428.1:c.175A>T
|
XP_024308196.1:p.Asn59Tyr
|
|
NM_001204527.2:c.388A>T
|
NP_001191456.1:p.Asn130Tyr
|
|
NM_006280.3:c.364A>T
MANE Select
|
NP_006271.1:p.Asn122Tyr
|
|