ENST00000573725.2:c.6741G>T
|
ENSP00000460849.2:p.Glu2247Asp
|
|
ENST00000703537.1:c.2669G>T
|
|
|
ENST00000703538.1:c.*6644G>T
|
ENSP00000515361.1:n.*6644G>T
|
|
ENST00000703539.1:n.3235G>T
|
|
|
ENST00000703540.1:c.6774G>T
|
ENSP00000515362.1:p.Glu2258Asp
|
|
ENST00000703541.1:c.6786G>T
|
ENSP00000515363.1:p.Glu2262Asp
|
|
ENST00000304992.11:c.6921G>T
MANE Select
|
ENSP00000304350.6:p.Glu2307Asp
|
|
ENST00000304992.10:c.6921G>T
|
ENSP00000304350.6:p.Glu2307Asp
|
|
ENST00000571958.1:c.163-43G>T
|
|
|
ENST00000572621.5:c.6921G>T
|
ENSP00000460348.1:p.Glu2307Asp
|
|
ENST00000572723.1:n.910G>T
|
|
|
NM_006445.3:c.6921G>T
|
NP_006436.3:p.Glu2307Asp
|
|
XM_024450537.1:c.6921G>T
|
XP_024306305.1:p.Glu2307Asp
|
|
NM_006445.4:c.6921G>T
MANE Select
|
NP_006436.3:p.Glu2307Asp
|
|