ENST00000249806.11:c.762C>T
MANE Select
|
ENSP00000249806.5:p.Phe254=
|
|
ENST00000562767.2:c.84-10686C>T
|
ENSP00000456336.1:n.84-10686C>T
|
|
ENST00000565471.6:c.303C>T
|
ENSP00000457384.1:p.Phe101=
|
|
ENST00000635747.1:c.*665C>T
|
ENSP00000490627.1:n.*665C>T
|
|
ENST00000636212.1:c.*432C>T
|
ENSP00000489851.1:n.*432C>T
|
|
ENST00000636674.1:n.1864C>T
|
|
|
ENST00000636964.1:n.2290C>T
|
|
|
ENST00000637054.1:c.198+10222C>T
|
ENSP00000490807.1:n.198+10222C>T
|
|
ENST00000637329.1:c.731C>T
|
|
|
ENST00000637450.1:c.*416C>T
|
ENSP00000490204.1:n.*416C>T
|
|
ENST00000637494.1:c.474C>T
|
ENSP00000490057.1:p.Phe158=
|
|
ENST00000637667.1:c.663C>T
|
ENSP00000489843.1:p.Phe221=
|
|
ENST00000637823.1:c.587C>T
|
|
|
ENST00000637888.1:c.198+10222C>T
|
ENSP00000490546.1:n.198+10222C>T
|
|
ENST00000638076.1:c.*365C>T
|
ENSP00000490373.1:n.*365C>T
|
|
ENST00000638144.1:n.405C>T
|
|
|
ENST00000646164.1:c.39-8633C>T
|
|
|
ENST00000249806.9:c.762C>T
|
ENSP00000249806.5:p.Phe254=
|
|
ENST00000538696.5:c.858C>T
|
ENSP00000445770.1:p.Phe286=
|
|
ENST00000562767.1:c.84-10686C>T
|
ENSP00000456336.1:n.84-10686C>T
|
|
ENST00000565471.5:c.303C>T
|
ENSP00000457384.1:p.Phe101=
|
|
ENST00000566347.5:c.573C>T
|
ENSP00000457783.1:p.Phe191=
|
|
ENST00000567060.5:c.*160C>T
|
ENSP00000454818.1:n.*160C>T
|
|
NM_017882.2:c.762C>T
|
NP_060352.1:p.Phe254=
|
|
NM_017882.3:c.762C>T
MANE Select
|
NP_060352.1:p.Phe254=
|
|