ENST00000269980.7:c.422A>G
MANE Select
|
ENSP00000269980.2:p.His141Arg
|
|
ENST00000269980.6:c.422A>G
|
ENSP00000269980.2:p.His141Arg
|
|
ENST00000457836.6:c.356A>G
|
ENSP00000416000.2:p.His119Arg
|
|
ENST00000538423.5:n.548A>G
|
|
|
ENST00000540732.3:c.524A>G
|
ENSP00000443246.1:p.His175Arg
|
|
ENST00000541315.1:c.229A>G
|
|
|
ENST00000542943.5:c.335A>G
|
ENSP00000440345.1:p.His112Arg
|
|
ENST00000595085.5:c.422A>G
|
ENSP00000471150.2:p.His141Arg
|
|
NM_000709.3:c.422A>G
|
NP_000700.1:p.His141Arg
|
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NM_001164783.1:c.422A>G
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NP_001158255.1:p.His141Arg
|
|
NM_000709.4:c.422A>G
MANE Select
|
NP_000700.1:p.His141Arg
|
|
NM_001164783.2:c.422A>G
|
NP_001158255.1:p.His141Arg
|
|