|
NM_006767.4:c.416A>G
MANE Select
|
NP_006758.2:p.Asp139Gly
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|
ENST00000646124.2:c.416A>G
MANE Select
|
ENSP00000496779.1:p.Asp139Gly
|
|
NM_006767.3:c.416A>G
|
NP_006758.2:p.Asp139Gly
|
|
ENST00000215739.12:c.416A>G
|
ENSP00000215739.8:p.Asp139Gly
|
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ENST00000414985.5:c.336A>G
|
ENSP00000397247.1:p.Gly112=
|
|
ENST00000443265.5:c.*115A>G
|
ENSP00000406466.1:n.*115A>G
|
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ENST00000479606.5:n.562A>G
|
|
|
ENST00000480895.1:n.112A>G
|
|
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ENST00000642151.1:c.247A>G
|
|
|
ENST00000644435.1:c.322A>G
|
|
|
ENST00000645935.1:c.359A>G
|
ENSP00000493479.1:p.Asp120Gly
|
|
ENST00000700578.1:c.416A>G
|
ENSP00000515073.1:p.Asp139Gly
|