ENST00000336098.8:c.1214T>C
MANE Select
|
ENSP00000336829.3:p.Met405Thr
|
|
ENST00000336098.7:c.1214T>C
|
ENSP00000336829.3:p.Met405Thr
|
|
ENST00000404648.7:c.1214T>C
|
ENSP00000384860.3:p.Met405Thr
|
|
ENST00000405164.5:c.1238T>C
|
ENSP00000384101.1:p.Met413Thr
|
|
ENST00000407946.5:c.1238T>C
|
ENSP00000384552.1:p.Met413Thr
|
|
ENST00000465913.1:n.762T>C
|
|
|
ENST00000492082.5:n.1756T>C
|
|
|
NM_000509.4:c.1214T>C
|
NP_000500.2:p.Met405Thr
|
|
NM_000509.5:c.1214T>C
|
NP_000500.2:p.Met405Thr
|
|
NM_021870.2:c.1214T>C
|
NP_068656.2:p.Met405Thr
|
|
NM_021870.3:c.1214T>C
MANE Select
|
NP_068656.2:p.Met405Thr
|
|
NM_000509.6:c.1214T>C
|
NP_000500.2:p.Met405Thr
|
|