ENST00000573725.2:c.6801T>A
|
ENSP00000460849.2:p.Ser2267=
|
|
ENST00000703537.1:c.2729T>A
|
|
|
ENST00000703538.1:c.*6704T>A
|
ENSP00000515361.1:n.*6704T>A
|
|
ENST00000703539.1:n.3295T>A
|
|
|
ENST00000703540.1:c.6834T>A
|
ENSP00000515362.1:p.Ser2278=
|
|
ENST00000703541.1:c.6846T>A
|
ENSP00000515363.1:p.Ser2282=
|
|
ENST00000304992.11:c.6981T>A
MANE Select
|
ENSP00000304350.6:p.Ser2327=
|
|
ENST00000304992.10:c.6981T>A
|
ENSP00000304350.6:p.Ser2327=
|
|
ENST00000571958.1:c.180T>A
|
|
|
ENST00000572621.5:c.6981T>A
|
ENSP00000460348.1:p.Ser2327=
|
|
NM_006445.3:c.6981T>A
|
NP_006436.3:p.Ser2327=
|
|
XM_024450537.1:c.6981T>A
|
XP_024306305.1:p.Ser2327=
|
|
NM_006445.4:c.6981T>A
MANE Select
|
NP_006436.3:p.Ser2327=
|
|