ENST00000295897.9:c.1082G>C
MANE Select
|
ENSP00000295897.4:p.Arg361Thr
|
|
ENST00000295897.8:c.1082G>C
|
ENSP00000295897.4:p.Arg361Thr
|
|
ENST00000401494.7:c.737G>C
|
ENSP00000384695.3:p.Arg246Thr
|
|
ENST00000415165.6:c.506G>C
|
ENSP00000401820.2:p.Arg169Thr
|
|
ENST00000476441.6:c.*361G>C
|
ENSP00000423727.1:n.*361G>C
|
|
ENST00000484992.1:n.402G>C
|
|
|
ENST00000503124.5:c.632G>C
|
ENSP00000421027.1:p.Arg211Thr
|
|
ENST00000504043.1:n.85G>C
|
|
|
ENST00000505649.5:n.768G>C
|
|
|
ENST00000509063.5:c.1082G>C
|
ENSP00000422784.1:p.Arg361Thr
|
|
ENST00000511370.1:c.615G>C
|
|
|
ENST00000621085.4:c.491-48G>C
|
ENSP00000483421.1:n.491-48G>C
|
|
ENST00000621628.4:c.487-44G>C
|
ENSP00000480485.1:n.487-44G>C
|
|
NM_000477.5:c.1082G>C
|
NP_000468.1:p.Arg361Thr
|
|
NM_000477.6:c.1082G>C
|
NP_000468.1:p.Arg361Thr
|
|
NM_000477.7:c.1082G>C
MANE Select
|
NP_000468.1:p.Arg361Thr
|
|