ENST00000330062.8:c.548A>G
MANE Select
|
ENSP00000331897.4:p.Asp183Gly
|
|
ENST00000330062.7:c.548A>G
|
ENSP00000331897.3:p.Asp183Gly
|
|
ENST00000540499.2:c.392A>G
|
ENSP00000446147.2:p.Asp131Gly
|
|
ENST00000559482.5:c.221A>G
|
ENSP00000453016.1:p.Asp74Gly
|
|
ENST00000560061.1:c.*173A>G
|
ENSP00000453254.1:n.*173A>G
|
|
NM_001289910.1:c.392A>G , LRG_611t1:c.392A>G
|
NP_001276839.1:p.Asp131Gly
|
|
NM_001290114.1:c.158A>G
|
NP_001277043.1:p.Asp53Gly
|
|
NM_002168.3:c.548A>G , LRG_611t2:c.548A>G
|
NP_002159.2:p.Asp183Gly
|
|
NM_001290114.2:c.158A>G
|
NP_001277043.1:p.Asp53Gly
|
|
NM_002168.4:c.548A>G
MANE Select
|
NP_002159.2:p.Asp183Gly
|
|