ENST00000253122.10:c.1312T>C
MANE Select
|
ENSP00000253122.5:p.Tyr438His
|
|
ENST00000253122.9:c.1312T>C
|
ENSP00000253122.5:p.Tyr438His
|
|
ENST00000413787.1:c.258-17T>C
|
ENSP00000400463.1:n.258-17T>C
|
|
ENST00000430077.6:c.967T>C
|
ENSP00000403041.2:p.Tyr323His
|
|
ENST00000442457.1:c.366T>C
|
|
|
ENST00000485324.1:n.1457T>C
|
|
|
NM_001142805.1:c.1282T>C
|
NP_001136277.1:p.Tyr428His
|
|
NM_001142806.1:c.967T>C
|
NP_001136278.1:p.Tyr323His
|
|
NM_005629.3:c.1312T>C
|
NP_005620.1:p.Tyr438His
|
|
NM_005629.4:c.1312T>C
MANE Select
|
NP_005620.1:p.Tyr438His
|
|
NM_001142805.2:c.1282T>C
|
NP_001136277.1:p.Tyr428His
|
|