ENST00000368305.9:c.117C>G
MANE Select
|
ENSP00000357288.4:p.Asp39Glu
|
|
ENST00000368302.3:c.117C>G
|
ENSP00000357285.3:p.Asp39Glu
|
|
ENST00000368304.9:c.117C>G
|
ENSP00000357287.5:p.Asp39Glu
|
|
ENST00000368305.8:c.117C>G
|
ENSP00000357288.4:p.Asp39Glu
|
|
ENST00000487106.5:n.227C>G
|
|
|
ENST00000489664.1:n.186C>G
|
|
|
NM_001145264.1:c.117C>G
|
NP_001138736.1:p.Asp39Glu
|
|
NM_014017.3:c.117C>G , LRG_81t1:c.117C>G
|
NP_054736.1:p.Asp39Glu
|
|
NM_001145264.2:c.117C>G
|
NP_001138736.1:p.Asp39Glu
|
|
NM_014017.4:c.117C>G
MANE Select
|
NP_054736.1:p.Asp39Glu
|
|