ENST00000395925.8:c.*1080G=
MANE Select
|
ENSP00000379258.3:n.*1080G=
|
|
ENST00000677288.1:c.*1080G=
|
ENSP00000503986.1:n.*1080G=
|
|
ENST00000677605.1:c.*1080G=
|
ENSP00000503743.1:n.*1080G=
|
|
ENST00000678429.1:c.*1080G=
|
ENSP00000502957.1:n.*1080G=
|
|
ENST00000395925.7:c.*1080G=
|
ENSP00000379258.3:n.*1080G=
|
|
NM_000168.5:c.*1080G=
|
NP_000159.3:n.*1080G=
|
|
XM_005249703.1:c.*1080G=
|
XP_005249760.1:n.*1080G=
|
|
XM_005249704.2:c.*1080G=
|
XP_005249761.1:n.*1080G=
|
|
XM_011515272.1:c.*1080G=
|
XP_011513574.1:n.*1080G=
|
|
XM_011515273.1:c.*1080G=
|
XP_011513575.1:n.*1080G=
|
|
XM_011515274.1:c.*1080G=
|
XP_011513576.1:n.*1080G=
|
|
NM_000168.6:c.*1080G=
MANE Select
|
NP_000159.3:n.*1080G=
|
|