ENST00000553106.6:c.1118C>A
MANE Select
|
ENSP00000448059.1:p.Ala373Asp
|
|
ENST00000307000.7:c.1103C>A
|
ENSP00000303500.2:p.Ala368Asp
|
|
ENST00000549247.6:n.877C>A
|
|
|
ENST00000551114.2:n.780C>A
|
|
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ENST00000553106.5:c.1118C>A
|
ENSP00000448059.1:p.Ala373Asp
|
|
ENST00000635477.1:c.222C>A
|
|
|
ENST00000635528.1:n.633C>A
|
|
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NM_000277.1:c.1118C>A
|
NP_000268.1:p.Ala373Asp
|
|
XM_011538422.1:c.1061C>A
|
XP_011536724.1:p.Ala354Asp
|
|
NM_000277.2:c.1118C>A
|
NP_000268.1:p.Ala373Asp
|
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NM_001354304.1:c.1118C>A
|
NP_001341233.1:p.Ala373Asp
|
|
NM_000277.3:c.1118C>A
MANE Select
|
NP_000268.1:p.Ala373Asp
|
|
NM_001354304.2:c.1118C>A
|
NP_001341233.1:p.Ala373Asp
|
|