ENST00000286657.10:c.1600-162G=
MANE Select
|
ENSP00000286657.4:n.1600-162G=
|
|
ENST00000286657.8:c.1600-162G=
|
ENSP00000286657.4:n.1600-162G=
|
|
ENST00000622135.1:c.1600-162G=
|
ENSP00000480055.1:n.1600-162G=
|
|
NM_014243.2:c.1600-162G=
|
NP_055058.2:n.1600-162G=
|
|
XM_011532421.1:c.1543-162G=
|
XP_011530723.1:n.1543-162G=
|
|
XM_011532422.1:c.1516-162G=
|
XP_011530724.1:n.1516-162G=
|
|
XM_011532423.1:c.958-162G=
|
XP_011530725.1:n.958-162G=
|
|
XM_011532424.1:c.868-162G=
|
XP_011530726.1:n.868-162G=
|
|
XM_011532421.2:c.1543-162G=
|
XP_011530723.1:n.1543-162G=
|
|
XM_011532422.3:c.1516-162G=
|
XP_011530724.1:n.1516-162G=
|
|
NM_014243.3:c.1600-162G=
MANE Select
|
NP_055058.2:n.1600-162G=
|
|