NM_000732.6:c.418C>G
MANE Select
|
NP_000723.1:p.Gln140Glu
|
ENST00000300692.9:c.418C>G
MANE Select
|
ENSP00000300692.4:p.Gln140Glu
|
NM_000732.4:c.418C>G , LRG_37t1:c.418C>G
|
NP_000723.1:p.Gln140Glu
|
NM_001040651.1:c.286C>G
|
NP_001035741.1:p.Gln96Glu
|
NM_001040651.2:c.286C>G
|
NP_001035741.1:p.Gln96Glu
|
ENST00000300692.8:c.418C>G
|
ENSP00000300692.4:p.Gln140Glu
|
ENST00000392884.2:c.286C>G
|
ENSP00000376622.2:p.Gln96Glu
|
ENST00000526561.1:n.91C>G
|
|
ENST00000529594.5:c.199C>G
|
ENSP00000437335.1:p.Gln67Glu
|
ENST00000534687.5:c.299C>G
|
|
ENST00000695666.1:n.1185C>G
|
|
ENST00000695667.1:n.703C>G
|
|