ENST00000295897.9:c.1676A>G
MANE Select
|
ENSP00000295897.4:p.His559Arg
|
|
ENST00000295897.8:c.1676A>G
|
ENSP00000295897.4:p.His559Arg
|
|
ENST00000401494.7:c.1331A>G
|
ENSP00000384695.3:p.His444Arg
|
|
ENST00000415165.6:c.1100A>G
|
ENSP00000401820.2:p.His367Arg
|
|
ENST00000476441.6:c.*955A>G
|
ENSP00000423727.1:n.*955A>G
|
|
ENST00000486939.1:n.330A>G
|
|
|
ENST00000503124.5:c.1226A>G
|
ENSP00000421027.1:p.His409Arg
|
|
ENST00000505649.5:n.1223A>G
|
|
|
ENST00000508932.5:n.175+75A>G
|
|
|
ENST00000509063.5:c.1676A>G
|
ENSP00000422784.1:p.His559Arg
|
|
ENST00000511370.1:c.1209A>G
|
|
|
ENST00000621085.4:c.1037A>G
|
ENSP00000483421.1:p.His346Arg
|
|
ENST00000621628.4:c.1037A>G
|
ENSP00000480485.1:p.His346Arg
|
|
NM_000477.5:c.1676A>G
|
NP_000468.1:p.His559Arg
|
|
NM_000477.6:c.1676A>G
|
NP_000468.1:p.His559Arg
|
|
NM_000477.7:c.1676A>G
MANE Select
|
NP_000468.1:p.His559Arg
|
|