ENST00000336906.6:c.437A>T
MANE Select
|
ENSP00000338082.4:p.Tyr146Phe
|
|
ENST00000380252.6:c.272A>T
|
ENSP00000369602.2:p.Tyr91Phe
|
|
ENST00000642908.1:c.315+1008A>T
|
ENSP00000495346.1:n.315+1008A>T
|
|
ENST00000647543.1:c.378+59A>T
|
ENSP00000496470.1:n.378+59A>T
|
|
ENST00000336906.4:c.437A>T
|
ENSP00000338082.4:p.Tyr146Phe
|
|
ENST00000380252.5:c.407A>T
|
ENSP00000369602.1:p.Tyr136Phe
|
|
ENST00000380259.6:c.437A>T
|
ENSP00000369609.2:p.Tyr146Phe
|
|
ENST00000620888.4:c.315+1008A>T
|
ENSP00000479637.1:n.315+1008A>T
|
|
NM_000184.2:c.437A>T
|
NP_000175.1:p.Tyr146Phe
|
|
NM_000184.3:c.437A>T
MANE Select
|
NP_000175.1:p.Tyr146Phe
|
|