ENST00000295897.9:c.434A>C
MANE Select
|
ENSP00000295897.4:p.Asp145Ala
|
|
ENST00000295897.8:c.434A>C
|
ENSP00000295897.4:p.Asp145Ala
|
|
ENST00000401494.7:c.138-598A>C
|
ENSP00000384695.3:n.138-598A>C
|
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ENST00000415165.6:c.138-3239A>C
|
ENSP00000401820.2:n.138-3239A>C
|
|
ENST00000441319.5:c.440A>C
|
ENSP00000392541.1:p.Asp147Ala
|
|
ENST00000476441.6:c.80-598A>C
|
ENSP00000423727.1:n.80-598A>C
|
|
ENST00000503124.5:c.33-598A>C
|
ENSP00000421027.1:n.33-598A>C
|
|
ENST00000505649.5:n.120A>C
|
|
|
ENST00000509063.5:c.434A>C
|
ENSP00000422784.1:p.Asp145Ala
|
|
ENST00000510166.5:n.470A>C
|
|
|
ENST00000514786.1:n.403A>C
|
|
|
ENST00000515133.5:n.475A>C
|
|
|
ENST00000621085.4:c.434A>C
|
ENSP00000483421.1:p.Asp145Ala
|
|
ENST00000621628.4:c.434A>C
|
ENSP00000480485.1:p.Asp145Ala
|
|
NM_000477.5:c.434A>C
|
NP_000468.1:p.Asp145Ala
|
|
NM_000477.6:c.434A>C
|
NP_000468.1:p.Asp145Ala
|
|
NM_000477.7:c.434A>C
MANE Select
|
NP_000468.1:p.Asp145Ala
|
|