ENST00000295897.9:c.207A>G
MANE Select
|
ENSP00000295897.4:p.Glu69=
|
|
ENST00000295897.8:c.207A>G
|
ENSP00000295897.4:p.Glu69=
|
|
ENST00000401494.7:c.137+1525A>G
|
ENSP00000384695.3:n.137+1525A>G
|
|
ENST00000415165.6:c.137+1525A>G
|
ENSP00000401820.2:n.137+1525A>G
|
|
ENST00000441319.5:c.213A>G
|
ENSP00000392541.1:p.Glu71=
|
|
ENST00000476441.6:c.79+2292A>G
|
ENSP00000423727.1:n.79+2292A>G
|
|
ENST00000503124.5:c.-32A>G
|
ENSP00000421027.1:n.-32A>G
|
|
ENST00000509063.5:c.207A>G
|
ENSP00000422784.1:p.Glu69=
|
|
ENST00000510166.5:n.243A>G
|
|
|
ENST00000514786.1:n.176A>G
|
|
|
ENST00000515133.5:n.248A>G
|
|
|
ENST00000621085.4:c.207A>G
|
ENSP00000483421.1:p.Glu69=
|
|
ENST00000621628.4:c.207A>G
|
ENSP00000480485.1:p.Glu69=
|
|
NM_000477.5:c.207A>G
|
NP_000468.1:p.Glu69=
|
|
NM_000477.6:c.207A>G
|
NP_000468.1:p.Glu69=
|
|
NM_000477.7:c.207A>G
MANE Select
|
NP_000468.1:p.Glu69=
|
|