ENST00000253122.10:c.1326A>G
MANE Select
|
ENSP00000253122.5:p.Gln442=
|
|
ENST00000253122.9:c.1326A>G
|
ENSP00000253122.5:p.Gln442=
|
|
ENST00000413787.1:c.258-3A>G
|
ENSP00000400463.1:n.258-3A>G
|
|
ENST00000430077.6:c.981A>G
|
ENSP00000403041.2:p.Gln327=
|
|
ENST00000442457.1:c.380A>G
|
|
|
ENST00000485324.1:n.1471A>G
|
|
|
NM_001142805.1:c.1296A>G
|
NP_001136277.1:p.Gln432=
|
|
NM_001142806.1:c.981A>G
|
NP_001136278.1:p.Gln327=
|
|
NM_005629.3:c.1326A>G
|
NP_005620.1:p.Gln442=
|
|
NM_005629.4:c.1326A>G
MANE Select
|
NP_005620.1:p.Gln442=
|
|
NM_001142805.2:c.1296A>G
|
NP_001136277.1:p.Gln432=
|
|