NM_000732.6:c.412G>A
MANE Select
|
NP_000723.1:p.Asp138Asn
|
ENST00000300692.9:c.412G>A
MANE Select
|
ENSP00000300692.4:p.Asp138Asn
|
NM_000732.4:c.412G>A , LRG_37t1:c.412G>A
|
NP_000723.1:p.Asp138Asn
|
NM_001040651.1:c.280G>A
|
NP_001035741.1:p.Asp94Asn
|
NM_001040651.2:c.280G>A
|
NP_001035741.1:p.Asp94Asn
|
ENST00000300692.8:c.412G>A
|
ENSP00000300692.4:p.Asp138Asn
|
ENST00000392884.2:c.280G>A
|
ENSP00000376622.2:p.Asp94Asn
|
ENST00000526561.1:n.85G>A
|
|
ENST00000529594.5:c.193G>A
|
ENSP00000437335.1:p.Asp65Asn
|
ENST00000534687.5:c.293G>A
|
|
ENST00000695666.1:n.1179G>A
|
|
ENST00000695667.1:n.697G>A
|
|