ENST00000336906.6:c.281G>A
MANE Select
|
ENSP00000338082.4:p.Cys94Tyr
|
|
ENST00000380252.6:c.116G>A
|
ENSP00000369602.2:p.Cys39Tyr
|
|
ENST00000642908.1:c.281G>A
|
ENSP00000495346.1:p.Cys94Tyr
|
|
ENST00000647543.1:c.281G>A
|
ENSP00000496470.1:p.Cys94Tyr
|
|
ENST00000336906.4:c.281G>A
|
ENSP00000338082.4:p.Cys94Tyr
|
|
ENST00000380252.5:c.251G>A
|
ENSP00000369602.1:p.Cys84Tyr
|
|
ENST00000380259.6:c.281G>A
|
ENSP00000369609.2:p.Cys94Tyr
|
|
ENST00000444587.1:c.*150G>A
|
ENSP00000488218.1:n.*150G>A
|
|
ENST00000620888.4:c.281G>A
|
ENSP00000479637.1:p.Cys94Tyr
|
|
ENST00000624109.1:c.74C>T
|
ENSP00000485458.1:p.Thr25Ile
|
|
NM_000184.2:c.281G>A
|
NP_000175.1:p.Cys94Tyr
|
|
NM_000184.3:c.281G>A
MANE Select
|
NP_000175.1:p.Cys94Tyr
|
|