ENST00000295897.9:c.1463A>G
MANE Select
|
ENSP00000295897.4:p.His488Arg
|
|
ENST00000295897.8:c.1463A>G
|
ENSP00000295897.4:p.His488Arg
|
|
ENST00000401494.7:c.1118A>G
|
ENSP00000384695.3:p.His373Arg
|
|
ENST00000415165.6:c.887A>G
|
ENSP00000401820.2:p.His296Arg
|
|
ENST00000476441.6:c.*742A>G
|
ENSP00000423727.1:n.*742A>G
|
|
ENST00000486939.1:n.117A>G
|
|
|
ENST00000503124.5:c.1013A>G
|
ENSP00000421027.1:p.His338Arg
|
|
ENST00000505649.5:n.1010A>G
|
|
|
ENST00000509063.5:c.1463A>G
|
ENSP00000422784.1:p.His488Arg
|
|
ENST00000511370.1:c.996A>G
|
|
|
ENST00000621085.4:c.824A>G
|
ENSP00000483421.1:p.His275Arg
|
|
ENST00000621628.4:c.824A>G
|
ENSP00000480485.1:p.His275Arg
|
|
NM_000477.5:c.1463A>G
|
NP_000468.1:p.His488Arg
|
|
NM_000477.6:c.1463A>G
|
NP_000468.1:p.His488Arg
|
|
NM_000477.7:c.1463A>G
MANE Select
|
NP_000468.1:p.His488Arg
|
|