ENST00000295897.9:c.270+396T>C
MANE Select
|
ENSP00000295897.4:n.270+396T>C
|
|
ENST00000295897.8:c.270+396T>C
|
ENSP00000295897.4:n.270+396T>C
|
|
ENST00000401494.7:c.137+1984T>C
|
ENSP00000384695.3:n.137+1984T>C
|
|
ENST00000415165.6:c.137+1984T>C
|
ENSP00000401820.2:n.137+1984T>C
|
|
ENST00000441319.5:c.276+396T>C
|
ENSP00000392541.1:n.276+396T>C
|
|
ENST00000476441.6:c.80-2198T>C
|
ENSP00000423727.1:n.80-2198T>C
|
|
ENST00000503124.5:c.32+396T>C
|
ENSP00000421027.1:n.32+396T>C
|
|
ENST00000509063.5:c.270+396T>C
|
ENSP00000422784.1:n.270+396T>C
|
|
ENST00000510166.5:n.306+396T>C
|
|
|
ENST00000514786.1:n.239+396T>C
|
|
|
ENST00000515133.5:n.311+396T>C
|
|
|
ENST00000621085.4:c.270+396T>C
|
ENSP00000483421.1:n.270+396T>C
|
|
ENST00000621628.4:c.270+396T>C
|
ENSP00000480485.1:n.270+396T>C
|
|
NM_000477.5:c.270+396T>C
|
NP_000468.1:n.270+396T>C
|
|
NM_000477.6:c.270+396T>C
|
NP_000468.1:n.270+396T>C
|
|
NM_000477.7:c.270+396T>C
MANE Select
|
NP_000468.1:n.270+396T>C
|
|