ENST00000378802.5:c.1161G>T
MANE Select
|
ENSP00000368079.4:p.Glu387Asp
|
|
ENST00000378802.4:c.1161G>T
|
ENSP00000368079.4:p.Glu387Asp
|
|
ENST00000502665.1:n.396G>T
|
|
|
ENST00000507209.5:n.5859G>T
|
|
|
ENST00000513354.5:n.251G>T
|
|
|
NM_207352.3:c.1161G>T
|
NP_997235.3:p.Glu387Asp
|
|
XM_005262935.2:c.1161G>T
|
XP_005262992.1:p.Glu387Asp
|
|
XM_006714184.2:c.765G>T
|
XP_006714247.1:p.Glu255Asp
|
|
XM_005262935.4:c.1161G>T
|
XP_005262992.1:p.Glu387Asp
|
|
XM_017008037.1:c.765G>T
|
XP_016863526.1:p.Glu255Asp
|
|
NM_207352.4:c.1161G>T
MANE Select
|
NP_997235.3:p.Glu387Asp
|
|