ENST00000371486.4:c.236A>C
MANE Select
|
ENSP00000360541.3:p.Lys79Thr
|
|
ENST00000468572.2:n.321A>C
|
|
|
ENST00000635862.1:c.236A>C
|
ENSP00000490867.1:p.Lys79Thr
|
|
ENST00000635888.1:c.*222A>C
|
ENSP00000490042.1:n.*222A>C
|
|
ENST00000636239.1:c.233+1526A>C
|
ENSP00000490066.1:n.233+1526A>C
|
|
ENST00000636673.1:n.2549A>C
|
|
|
ENST00000636867.1:c.236A>C
|
ENSP00000489631.1:p.Lys79Thr
|
|
ENST00000636891.1:c.236A>C
|
ENSP00000490399.1:p.Lys79Thr
|
|
ENST00000636935.1:c.236A>C
|
ENSP00000489757.1:p.Lys79Thr
|
|
ENST00000637252.1:c.236A>C
|
ENSP00000490492.1:p.Lys79Thr
|
|
ENST00000638135.1:c.152+5230A>C
|
ENSP00000489756.1:n.152+5230A>C
|
|
ENST00000371486.3:c.236A>C
|
ENSP00000360541.3:p.Lys79Thr
|
|
ENST00000468572.1:n.321A>C
|
|
|
NM_000098.2:c.236A>C
|
NP_000089.1:p.Lys79Thr
|
|
XM_005270484.1:c.236A>C
|
XP_005270541.1:p.Lys79Thr
|
|
NM_001330589.1:c.236A>C
|
NP_001317518.1:p.Lys79Thr
|
|
NM_000098.3:c.236A>C
MANE Select
|
NP_000089.1:p.Lys79Thr
|
|
NM_001330589.2:c.236A>C
|
NP_001317518.1:p.Lys79Thr
|
|