ENST00000361669.7:c.1325-23385T=
MANE Select
|
ENSP00000355316.2:n.1325-23385T=
|
|
ENST00000361669.6:c.1325-23385T=
|
ENSP00000355316.2:n.1325-23385T=
|
|
ENST00000439827.1:c.1324+28338T=
|
ENSP00000398767.1:n.1324+28338T=
|
|
NM_000840.2:c.1325-23385T=
|
NP_000831.2:n.1325-23385T=
|
|
XM_011516088.1:c.1324+28338T=
|
XP_011514390.1:n.1324+28338T=
|
|
XM_011516089.1:c.*207T=
|
XP_011514391.1:n.*207T=
|
|
XM_011516090.1:c.1325-17568T=
|
XP_011514392.1:n.1325-17568T=
|
|
NM_001363522.1:c.1324+28338T=
|
NP_001350451.1:n.1324+28338T=
|
|
NM_000840.3:c.1325-23385T=
MANE Select
|
NP_000831.2:n.1325-23385T=
|
|
NM_001363522.2:c.1324+28338T=
|
NP_001350451.1:n.1324+28338T=
|
|