ENST00000340855.11:c.1032A>C
MANE Select
|
ENSP00000339801.6:p.Glu344Asp
|
|
ENST00000651111.1:c.399A>C
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ENSP00000498395.1:p.Glu133Asp
|
|
ENST00000340855.10:c.1032A>C
|
ENSP00000339801.6:p.Glu344Asp
|
|
ENST00000422081.6:c.399A>C
|
ENSP00000477056.1:p.Glu133Asp
|
|
ENST00000441880.1:n.139A>C
|
|
|
NM_000202.6:c.1032A>C
|
NP_000193.1:p.Glu344Asp
|
|
NM_001166550.2:c.762A>C
|
NP_001160022.1:p.Glu254Asp
|
|
NM_000202.7:c.1032A>C
|
NP_000193.1:p.Glu344Asp
|
|
NM_001166550.3:c.762A>C
|
NP_001160022.1:p.Glu254Asp
|
|
NM_000202.8:c.1032A>C
MANE Select
|
NP_000193.1:p.Glu344Asp
|
|
NM_001166550.4:c.762A>C
|
NP_001160022.1:p.Glu254Asp
|
|