ENST00000395925.8:c.3223C>T
MANE Select
|
ENSP00000379258.3:p.Leu1075=
|
|
ENST00000677288.1:c.3049C>T
|
ENSP00000503986.1:p.Leu1017=
|
|
ENST00000677605.1:c.3223C>T
|
ENSP00000503743.1:p.Leu1075=
|
|
ENST00000678429.1:c.3223C>T
|
ENSP00000502957.1:p.Leu1075=
|
|
ENST00000395925.7:c.3223C>T
|
ENSP00000379258.3:p.Leu1075=
|
|
ENST00000479210.1:n.3200C>T
|
|
|
NM_000168.5:c.3223C>T
|
NP_000159.3:p.Leu1075=
|
|
XM_005249703.1:c.3223C>T
|
XP_005249760.1:p.Leu1075=
|
|
XM_005249704.2:c.3223C>T
|
XP_005249761.1:p.Leu1075=
|
|
XM_011515272.1:c.3223C>T
|
XP_011513574.1:p.Leu1075=
|
|
XM_011515273.1:c.3223C>T
|
XP_011513575.1:p.Leu1075=
|
|
XM_011515274.1:c.3046C>T
|
XP_011513576.1:p.Leu1016=
|
|
XM_011515274.2:c.3046C>T
|
XP_011513576.1:p.Leu1016=
|
|
XM_017011997.1:c.3220C>T
|
XP_016867486.1:p.Leu1074=
|
|
NM_000168.6:c.3223C>T
MANE Select
|
NP_000159.3:p.Leu1075=
|
|