ENST00000330062.8:c.569G>A
MANE Select
|
ENSP00000331897.4:p.Gly190Asp
|
|
ENST00000330062.7:c.569G>A
|
ENSP00000331897.3:p.Gly190Asp
|
|
ENST00000540499.2:c.413G>A
|
ENSP00000446147.2:p.Gly138Asp
|
|
ENST00000559482.5:c.242G>A
|
ENSP00000453016.1:p.Gly81Asp
|
|
ENST00000560061.1:c.*194G>A
|
ENSP00000453254.1:n.*194G>A
|
|
NM_001289910.1:c.413G>A , LRG_611t1:c.413G>A
|
NP_001276839.1:p.Gly138Asp
|
|
NM_001290114.1:c.179G>A
|
NP_001277043.1:p.Gly60Asp
|
|
NM_002168.3:c.569G>A , LRG_611t2:c.569G>A
|
NP_002159.2:p.Gly190Asp
|
|
NM_001290114.2:c.179G>A
|
NP_001277043.1:p.Gly60Asp
|
|
NM_002168.4:c.569G>A
MANE Select
|
NP_002159.2:p.Gly190Asp
|
|