ENST00000298910.12:c.6072C>T
MANE Select
|
ENSP00000298910.7:p.Cys2024=
|
|
ENST00000679360.1:c.*4981C>T
|
ENSP00000505368.1:n.*4981C>T
|
|
ENST00000679532.1:c.1846C>T
|
|
|
ENST00000680018.1:c.1517C>T
|
ENSP00000505347.1:n.1517C>T
|
|
ENST00000680422.1:c.1717C>T
|
|
|
ENST00000680425.1:c.1239C>T
|
ENSP00000506459.1:n.1239C>T
|
|
ENST00000680453.1:c.1529C>T
|
|
|
ENST00000680790.1:c.5817C>T
|
ENSP00000505335.1:p.Cys1939=
|
|
ENST00000681136.1:n.2056C>T
|
|
|
ENST00000681696.1:c.1755C>T
|
ENSP00000505871.1:p.Cys585=
|
|
ENST00000298910.11:c.6072C>T
|
ENSP00000298910.7:p.Cys2024=
|
|
ENST00000430804.5:c.3368C>T
|
|
|
ENST00000479187.5:n.2753C>T
|
|
|
NM_198578.3:c.6072C>T
|
NP_940980.3:p.Cys2024=
|
|
XM_005268629.2:c.6072C>T
|
XP_005268686.1:p.Cys2024=
|
|
XM_011537877.1:c.6072C>T
|
XP_011536179.1:p.Cys2024=
|
|
XM_011537878.1:c.6072C>T
|
XP_011536180.1:p.Cys2024=
|
|
XM_011537879.1:c.4869C>T
|
XP_011536181.1:p.Cys1623=
|
|
XM_005268629.4:c.6072C>T
|
XP_005268686.1:p.Cys2024=
|
|
XM_011537877.3:c.6072C>T
|
XP_011536179.1:p.Cys2024=
|
|
XM_017018787.1:c.2988C>T
|
XP_016874276.1:p.Cys996=
|
|
XM_017018788.2:c.2334C>T
|
XP_016874277.1:p.Cys778=
|
|
XM_024448833.1:c.4869C>T
|
XP_024304601.1:p.Cys1623=
|
|
NM_198578.4:c.6072C>T
MANE Select
|
NP_940980.4:p.Cys2024=
|
|