ENST00000573725.2:c.6495G>T
|
ENSP00000460849.2:p.Leu2165=
|
|
ENST00000703537.1:c.2423G>T
|
|
|
ENST00000703538.1:c.*6398G>T
|
ENSP00000515361.1:n.*6398G>T
|
|
ENST00000703539.1:n.2989G>T
|
|
|
ENST00000703540.1:c.6528G>T
|
ENSP00000515362.1:p.Leu2176=
|
|
ENST00000703541.1:c.6540G>T
|
ENSP00000515363.1:p.Leu2180=
|
|
ENST00000304992.11:c.6675G>T
MANE Select
|
ENSP00000304350.6:p.Leu2225=
|
|
ENST00000304992.10:c.6675G>T
|
ENSP00000304350.6:p.Leu2225=
|
|
ENST00000572621.5:c.6675G>T
|
ENSP00000460348.1:p.Leu2225=
|
|
ENST00000572723.1:n.664G>T
|
|
|
NM_006445.3:c.6675G>T
|
NP_006436.3:p.Leu2225=
|
|
XM_024450537.1:c.6675G>T
|
XP_024306305.1:p.Leu2225=
|
|
NM_006445.4:c.6675G>T
MANE Select
|
NP_006436.3:p.Leu2225=
|
|