ENST00000295897.9:c.879T>A
MANE Select
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ENSP00000295897.4:p.Asp293Glu
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ENST00000295897.8:c.879T>A
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ENSP00000295897.4:p.Asp293Glu
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ENST00000401494.7:c.534T>A
|
ENSP00000384695.3:p.Asp178Glu
|
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ENST00000415165.6:c.303T>A
|
ENSP00000401820.2:p.Asp101Glu
|
|
ENST00000476441.6:c.*158T>A
|
ENSP00000423727.1:n.*158T>A
|
|
ENST00000484992.1:n.199T>A
|
|
|
ENST00000503124.5:c.429T>A
|
ENSP00000421027.1:p.Asp143Glu
|
|
ENST00000505649.5:n.565T>A
|
|
|
ENST00000509063.5:c.879T>A
|
ENSP00000422784.1:p.Asp293Glu
|
|
ENST00000511370.1:c.412T>A
|
|
|
ENST00000621085.4:c.491-1651T>A
|
ENSP00000483421.1:n.491-1651T>A
|
|
ENST00000621628.4:c.487-1647T>A
|
ENSP00000480485.1:n.487-1647T>A
|
|
NM_000477.5:c.879T>A
|
NP_000468.1:p.Asp293Glu
|
|
NM_000477.6:c.879T>A
|
NP_000468.1:p.Asp293Glu
|
|
NM_000477.7:c.879T>A
MANE Select
|
NP_000468.1:p.Asp293Glu
|
|