ENST00000295897.9:c.1487G>C
MANE Select
|
ENSP00000295897.4:p.Arg496Thr
|
|
ENST00000295897.8:c.1487G>C
|
ENSP00000295897.4:p.Arg496Thr
|
|
ENST00000401494.7:c.1142G>C
|
ENSP00000384695.3:p.Arg381Thr
|
|
ENST00000415165.6:c.911G>C
|
ENSP00000401820.2:p.Arg304Thr
|
|
ENST00000476441.6:c.*766G>C
|
ENSP00000423727.1:n.*766G>C
|
|
ENST00000486939.1:n.141G>C
|
|
|
ENST00000503124.5:c.1037G>C
|
ENSP00000421027.1:p.Arg346Thr
|
|
ENST00000505649.5:n.1034G>C
|
|
|
ENST00000509063.5:c.1487G>C
|
ENSP00000422784.1:p.Arg496Thr
|
|
ENST00000511370.1:c.1020G>C
|
|
|
ENST00000621085.4:c.848G>C
|
ENSP00000483421.1:p.Arg283Thr
|
|
ENST00000621628.4:c.848G>C
|
ENSP00000480485.1:p.Arg283Thr
|
|
NM_000477.5:c.1487G>C
|
NP_000468.1:p.Arg496Thr
|
|
NM_000477.6:c.1487G>C
|
NP_000468.1:p.Arg496Thr
|
|
NM_000477.7:c.1487G>C
MANE Select
|
NP_000468.1:p.Arg496Thr
|
|