ENST00000295897.9:c.1485C>G
MANE Select
|
ENSP00000295897.4:p.Asp495Glu
|
|
ENST00000295897.8:c.1485C>G
|
ENSP00000295897.4:p.Asp495Glu
|
|
ENST00000401494.7:c.1140C>G
|
ENSP00000384695.3:p.Asp380Glu
|
|
ENST00000415165.6:c.909C>G
|
ENSP00000401820.2:p.Asp303Glu
|
|
ENST00000476441.6:c.*764C>G
|
ENSP00000423727.1:n.*764C>G
|
|
ENST00000486939.1:n.139C>G
|
|
|
ENST00000503124.5:c.1035C>G
|
ENSP00000421027.1:p.Asp345Glu
|
|
ENST00000505649.5:n.1032C>G
|
|
|
ENST00000509063.5:c.1485C>G
|
ENSP00000422784.1:p.Asp495Glu
|
|
ENST00000511370.1:c.1018C>G
|
|
|
ENST00000621085.4:c.846C>G
|
ENSP00000483421.1:p.Asp282Glu
|
|
ENST00000621628.4:c.846C>G
|
ENSP00000480485.1:p.Asp282Glu
|
|
NM_000477.5:c.1485C>G
|
NP_000468.1:p.Asp495Glu
|
|
NM_000477.6:c.1485C>G
|
NP_000468.1:p.Asp495Glu
|
|
NM_000477.7:c.1485C>G
MANE Select
|
NP_000468.1:p.Asp495Glu
|
|