ENST00000295897.9:c.1575G>C
MANE Select
|
ENSP00000295897.4:p.Glu525Asp
|
|
ENST00000295897.8:c.1575G>C
|
ENSP00000295897.4:p.Glu525Asp
|
|
ENST00000401494.7:c.1230G>C
|
ENSP00000384695.3:p.Glu410Asp
|
|
ENST00000415165.6:c.999G>C
|
ENSP00000401820.2:p.Glu333Asp
|
|
ENST00000476441.6:c.*854G>C
|
ENSP00000423727.1:n.*854G>C
|
|
ENST00000486939.1:n.229G>C
|
|
|
ENST00000503124.5:c.1125G>C
|
ENSP00000421027.1:p.Glu375Asp
|
|
ENST00000505649.5:n.1122G>C
|
|
|
ENST00000509063.5:c.1575G>C
|
ENSP00000422784.1:p.Glu525Asp
|
|
ENST00000511370.1:c.1108G>C
|
|
|
ENST00000621085.4:c.936G>C
|
ENSP00000483421.1:p.Glu312Asp
|
|
ENST00000621628.4:c.936G>C
|
ENSP00000480485.1:p.Glu312Asp
|
|
NM_000477.5:c.1575G>C
|
NP_000468.1:p.Glu525Asp
|
|
NM_000477.6:c.1575G>C
|
NP_000468.1:p.Glu525Asp
|
|
NM_000477.7:c.1575G>C
MANE Select
|
NP_000468.1:p.Glu525Asp
|
|