ENST00000295897.9:c.429G>T
MANE Select
|
ENSP00000295897.4:p.Glu143Asp
|
|
ENST00000295897.8:c.429G>T
|
ENSP00000295897.4:p.Glu143Asp
|
|
ENST00000401494.7:c.138-603G>T
|
ENSP00000384695.3:n.138-603G>T
|
|
ENST00000415165.6:c.138-3244G>T
|
ENSP00000401820.2:n.138-3244G>T
|
|
ENST00000441319.5:c.435G>T
|
ENSP00000392541.1:p.Glu145Asp
|
|
ENST00000476441.6:c.80-603G>T
|
ENSP00000423727.1:n.80-603G>T
|
|
ENST00000503124.5:c.33-603G>T
|
ENSP00000421027.1:n.33-603G>T
|
|
ENST00000505649.5:n.115G>T
|
|
|
ENST00000509063.5:c.429G>T
|
ENSP00000422784.1:p.Glu143Asp
|
|
ENST00000510166.5:n.465G>T
|
|
|
ENST00000514786.1:n.398G>T
|
|
|
ENST00000515133.5:n.470G>T
|
|
|
ENST00000621085.4:c.429G>T
|
ENSP00000483421.1:p.Glu143Asp
|
|
ENST00000621628.4:c.429G>T
|
ENSP00000480485.1:p.Glu143Asp
|
|
NM_000477.5:c.429G>T
|
NP_000468.1:p.Glu143Asp
|
|
NM_000477.6:c.429G>T
|
NP_000468.1:p.Glu143Asp
|
|
NM_000477.7:c.429G>T
MANE Select
|
NP_000468.1:p.Glu143Asp
|
|