ENST00000573725.2:c.6708A>G
|
ENSP00000460849.2:p.Leu2236=
|
|
ENST00000703537.1:c.2636A>G
|
|
|
ENST00000703538.1:c.*6611A>G
|
ENSP00000515361.1:n.*6611A>G
|
|
ENST00000703539.1:n.3202A>G
|
|
|
ENST00000703540.1:c.6741A>G
|
ENSP00000515362.1:p.Leu2247=
|
|
ENST00000703541.1:c.6753A>G
|
ENSP00000515363.1:p.Leu2251=
|
|
ENST00000304992.11:c.6888A>G
MANE Select
|
ENSP00000304350.6:p.Leu2296=
|
|
ENST00000304992.10:c.6888A>G
|
ENSP00000304350.6:p.Leu2296=
|
|
ENST00000571958.1:c.163-76A>G
|
|
|
ENST00000572621.5:c.6888A>G
|
ENSP00000460348.1:p.Leu2296=
|
|
ENST00000572723.1:n.877A>G
|
|
|
NM_006445.3:c.6888A>G
|
NP_006436.3:p.Leu2296=
|
|
XM_024450537.1:c.6888A>G
|
XP_024306305.1:p.Leu2296=
|
|
NM_006445.4:c.6888A>G
MANE Select
|
NP_006436.3:p.Leu2296=
|
|