ENST00000398603.6:c.337-211C>T
|
ENSP00000381604.1:n.337-211C>T
|
|
ENST00000398606.10:c.411C>T
MANE Select
|
ENSP00000381607.3:p.Asn137=
|
|
ENST00000646888.1:c.*127C>T
|
ENSP00000494477.1:n.*127C>T
|
|
ENST00000398603.5:c.337-211C>T
|
ENSP00000381604.1:n.337-211C>T
|
|
ENST00000398606.7:c.411C>T
|
ENSP00000381607.3:p.Asn137=
|
|
ENST00000467591.1:n.522C>T
|
|
|
ENST00000494593.1:n.1206C>T
|
|
|
ENST00000495996.1:c.75C>T
|
ENSP00000484686.1:p.Asn25=
|
|
ENST00000498765.5:c.474C>T
|
|
|
NM_000852.3:c.411C>T , LRG_723t1:c.411C>T
|
NP_000843.1:p.Asn137=
|
|
NM_000852.4:c.411C>T
MANE Select
|
NP_000843.1:p.Asn137=
|
|