ENST00000395925.8:c.936G>T
MANE Select
|
ENSP00000379258.3:p.Thr312=
|
|
ENST00000677288.1:c.759G>T
|
ENSP00000503986.1:p.Thr253=
|
|
ENST00000677605.1:c.936G>T
|
ENSP00000503743.1:p.Thr312=
|
|
ENST00000678429.1:c.936G>T
|
ENSP00000502957.1:p.Thr312=
|
|
ENST00000395925.7:c.936G>T
|
ENSP00000379258.3:p.Thr312=
|
|
ENST00000479210.1:n.913G>T
|
|
|
NM_000168.5:c.936G>T
|
NP_000159.3:p.Thr312=
|
|
XM_005249703.1:c.936G>T
|
XP_005249760.1:p.Thr312=
|
|
XM_005249704.2:c.936G>T
|
XP_005249761.1:p.Thr312=
|
|
XM_011515272.1:c.936G>T
|
XP_011513574.1:p.Thr312=
|
|
XM_011515273.1:c.936G>T
|
XP_011513575.1:p.Thr312=
|
|
XM_011515274.1:c.759G>T
|
XP_011513576.1:p.Thr253=
|
|
XM_011515274.2:c.759G>T
|
XP_011513576.1:p.Thr253=
|
|
XM_017011997.1:c.933G>T
|
XP_016867486.1:p.Thr311=
|
|
NM_000168.6:c.936G>T
MANE Select
|
NP_000159.3:p.Thr312=
|
|