ENST00000573725.2:c.6618T>A
|
ENSP00000460849.2:p.Arg2206=
|
|
ENST00000703537.1:c.2546T>A
|
|
|
ENST00000703538.1:c.*6521T>A
|
ENSP00000515361.1:n.*6521T>A
|
|
ENST00000703539.1:n.3112T>A
|
|
|
ENST00000703540.1:c.6651T>A
|
ENSP00000515362.1:p.Arg2217=
|
|
ENST00000703541.1:c.6663T>A
|
ENSP00000515363.1:p.Arg2221=
|
|
ENST00000304992.11:c.6798T>A
MANE Select
|
ENSP00000304350.6:p.Arg2266=
|
|
ENST00000304992.10:c.6798T>A
|
ENSP00000304350.6:p.Arg2266=
|
|
ENST00000571958.1:c.107T>A
|
|
|
ENST00000572621.5:c.6798T>A
|
ENSP00000460348.1:p.Arg2266=
|
|
ENST00000572723.1:n.787T>A
|
|
|
NM_006445.3:c.6798T>A
|
NP_006436.3:p.Arg2266=
|
|
XM_024450537.1:c.6798T>A
|
XP_024306305.1:p.Arg2266=
|
|
NM_006445.4:c.6798T>A
MANE Select
|
NP_006436.3:p.Arg2266=
|
|