ENST00000253122.10:c.1246G>T
MANE Select
|
ENSP00000253122.5:p.Asp416Tyr
|
|
ENST00000253122.9:c.1246G>T
|
ENSP00000253122.5:p.Asp416Tyr
|
|
ENST00000413787.1:c.258-195G>T
|
ENSP00000400463.1:n.258-195G>T
|
|
ENST00000430077.6:c.901G>T
|
ENSP00000403041.2:p.Asp301Tyr
|
|
ENST00000442457.1:c.300G>T
|
|
|
ENST00000457723.1:c.230G>T
|
ENSP00000394742.1:p.Arg77Leu
|
|
ENST00000485324.1:n.1279G>T
|
|
|
NM_001142805.1:c.1216G>T
|
NP_001136277.1:p.Asp406Tyr
|
|
NM_001142806.1:c.901G>T
|
NP_001136278.1:p.Asp301Tyr
|
|
NM_005629.3:c.1246G>T
|
NP_005620.1:p.Asp416Tyr
|
|
NM_005629.4:c.1246G>T
MANE Select
|
NP_005620.1:p.Asp416Tyr
|
|
NM_001142805.2:c.1216G>T
|
NP_001136277.1:p.Asp406Tyr
|
|