ENST00000265512.12:c.879A>T
MANE Select
|
ENSP00000265512.7:p.Gly293=
|
|
ENST00000265512.11:c.879A>T
|
ENSP00000265512.7:p.Gly293=
|
|
ENST00000505590.5:c.936A>T
|
ENSP00000425416.1:p.Gly312=
|
|
ENST00000506705.5:c.*853A>T
|
ENSP00000426667.1:n.*853A>T
|
|
ENST00000508393.5:c.936A>T
|
ENSP00000424630.1:p.Gly312=
|
|
ENST00000509471.5:c.334-577A>T
|
ENSP00000424583.1:n.334-577A>T
|
|
ENST00000629236.2:c.879A>T
|
ENSP00000486450.1:p.Gly293=
|
|
NM_000670.3:c.879A>T
|
NP_000661.2:p.Gly293=
|
|
NM_000670.4:c.879A>T
|
NP_000661.2:p.Gly293=
|
|
NM_001306171.1:c.936A>T
|
NP_001293100.1:p.Gly312=
|
|
NM_001306172.1:c.936A>T
|
NP_001293101.1:p.Gly312=
|
|
NR_037884.1:n.429-6246T>A
|
|
|
XR_938685.1:n.1107A>T
|
|
|
XR_938686.1:n.1098A>T
|
|
|
XR_938687.1:n.971A>T
|
|
|
NM_000670.5:c.879A>T
MANE Select
|
NP_000661.2:p.Gly293=
|
|
NM_001306171.2:c.936A>T
|
NP_001293100.1:p.Gly312=
|
|
NM_001306172.2:c.936A>T
|
NP_001293101.1:p.Gly312=
|
|