ENST00000398603.6:c.378C>T
|
ENSP00000381604.1:p.Ile126=
|
|
ENST00000398606.10:c.486C>T
MANE Select
|
ENSP00000381607.3:p.Ile162=
|
|
ENST00000646888.1:c.*202C>T
|
ENSP00000494477.1:n.*202C>T
|
|
ENST00000398603.5:c.378C>T
|
ENSP00000381604.1:p.Ile126=
|
|
ENST00000398606.7:c.486C>T
|
ENSP00000381607.3:p.Ile162=
|
|
ENST00000467591.1:n.597C>T
|
|
|
ENST00000494593.1:n.1458C>T
|
|
|
ENST00000495996.1:c.212C>T
|
ENSP00000484686.1:n.212C>T
|
|
ENST00000498765.5:c.549C>T
|
|
|
NM_000852.3:c.486C>T , LRG_723t1:c.486C>T
|
NP_000843.1:p.Ile162=
|
|
NM_000852.4:c.486C>T
MANE Select
|
NP_000843.1:p.Ile162=
|
|