ENST00000295897.9:c.1184C>A
MANE Select
|
ENSP00000295897.4:p.Ala395Asp
|
|
ENST00000295897.8:c.1184C>A
|
ENSP00000295897.4:p.Ala395Asp
|
|
ENST00000401494.7:c.839C>A
|
ENSP00000384695.3:p.Ala280Asp
|
|
ENST00000415165.6:c.608C>A
|
ENSP00000401820.2:p.Ala203Asp
|
|
ENST00000476441.6:c.*463C>A
|
ENSP00000423727.1:n.*463C>A
|
|
ENST00000484992.1:n.504C>A
|
|
|
ENST00000503124.5:c.734C>A
|
ENSP00000421027.1:p.Ala245Asp
|
|
ENST00000504043.1:n.187C>A
|
|
|
ENST00000505649.5:n.870C>A
|
|
|
ENST00000509063.5:c.1184C>A
|
ENSP00000422784.1:p.Ala395Asp
|
|
ENST00000511370.1:c.717C>A
|
|
|
ENST00000621085.4:c.545C>A
|
ENSP00000483421.1:p.Ala182Asp
|
|
ENST00000621628.4:c.545C>A
|
ENSP00000480485.1:p.Ala182Asp
|
|
NM_000477.5:c.1184C>A
|
NP_000468.1:p.Ala395Asp
|
|
NM_000477.6:c.1184C>A
|
NP_000468.1:p.Ala395Asp
|
|
NM_000477.7:c.1184C>A
MANE Select
|
NP_000468.1:p.Ala395Asp
|
|