ENST00000253122.10:c.1340T>A
MANE Select
|
ENSP00000253122.5:p.Val447Glu
|
|
ENST00000253122.9:c.1340T>A
|
ENSP00000253122.5:p.Val447Glu
|
|
ENST00000413787.1:c.269T>A
|
ENSP00000400463.1:p.Val90Glu
|
|
ENST00000430077.6:c.995T>A
|
ENSP00000403041.2:p.Val332Glu
|
|
ENST00000442457.1:c.394T>A
|
|
|
ENST00000485324.1:n.1485T>A
|
|
|
NM_001142805.1:c.1310T>A
|
NP_001136277.1:p.Val437Glu
|
|
NM_001142806.1:c.995T>A
|
NP_001136278.1:p.Val332Glu
|
|
NM_005629.3:c.1340T>A
|
NP_005620.1:p.Val447Glu
|
|
NM_005629.4:c.1340T>A
MANE Select
|
NP_005620.1:p.Val447Glu
|
|
NM_001142805.2:c.1310T>A
|
NP_001136277.1:p.Val437Glu
|
|