ENST00000295897.9:c.904T>C
MANE Select
|
ENSP00000295897.4:p.Cys302Arg
|
|
ENST00000295897.8:c.904T>C
|
ENSP00000295897.4:p.Cys302Arg
|
|
ENST00000401494.7:c.559T>C
|
ENSP00000384695.3:p.Cys187Arg
|
|
ENST00000415165.6:c.328T>C
|
ENSP00000401820.2:p.Cys110Arg
|
|
ENST00000476441.6:c.*183T>C
|
ENSP00000423727.1:n.*183T>C
|
|
ENST00000484992.1:n.224T>C
|
|
|
ENST00000503124.5:c.454T>C
|
ENSP00000421027.1:p.Cys152Arg
|
|
ENST00000505649.5:n.590T>C
|
|
|
ENST00000509063.5:c.904T>C
|
ENSP00000422784.1:p.Cys302Arg
|
|
ENST00000511370.1:c.437T>C
|
|
|
ENST00000621085.4:c.491-1626T>C
|
ENSP00000483421.1:n.491-1626T>C
|
|
ENST00000621628.4:c.487-1622T>C
|
ENSP00000480485.1:n.487-1622T>C
|
|
NM_000477.5:c.904T>C
|
NP_000468.1:p.Cys302Arg
|
|
NM_000477.6:c.904T>C
|
NP_000468.1:p.Cys302Arg
|
|
NM_000477.7:c.904T>C
MANE Select
|
NP_000468.1:p.Cys302Arg
|
|