ENST00000298910.12:c.6000G>T
MANE Select
|
ENSP00000298910.7:p.Val2000=
|
|
ENST00000679360.1:c.*4909G>T
|
ENSP00000505368.1:n.*4909G>T
|
|
ENST00000679532.1:c.1774G>T
|
|
|
ENST00000680018.1:c.1445G>T
|
ENSP00000505347.1:n.1445G>T
|
|
ENST00000680422.1:c.1645G>T
|
|
|
ENST00000680425.1:c.1167G>T
|
ENSP00000506459.1:n.1167G>T
|
|
ENST00000680453.1:c.1457G>T
|
|
|
ENST00000680790.1:c.5745G>T
|
ENSP00000505335.1:p.Val1915=
|
|
ENST00000681136.1:n.1984G>T
|
|
|
ENST00000681696.1:c.1683G>T
|
ENSP00000505871.1:p.Val561=
|
|
ENST00000298910.11:c.6000G>T
|
ENSP00000298910.7:p.Val2000=
|
|
ENST00000430804.5:c.3296G>T
|
|
|
ENST00000479187.5:n.2681G>T
|
|
|
NM_198578.3:c.6000G>T
|
NP_940980.3:p.Val2000=
|
|
XM_005268629.2:c.6000G>T
|
XP_005268686.1:p.Val2000=
|
|
XM_011537877.1:c.6000G>T
|
XP_011536179.1:p.Val2000=
|
|
XM_011537878.1:c.6000G>T
|
XP_011536180.1:p.Val2000=
|
|
XM_011537879.1:c.4797G>T
|
XP_011536181.1:p.Val1599=
|
|
XM_005268629.4:c.6000G>T
|
XP_005268686.1:p.Val2000=
|
|
XM_011537877.3:c.6000G>T
|
XP_011536179.1:p.Val2000=
|
|
XM_017018787.1:c.2916G>T
|
XP_016874276.1:p.Val972=
|
|
XM_017018788.2:c.2262G>T
|
XP_016874277.1:p.Val754=
|
|
XM_024448833.1:c.4797G>T
|
XP_024304601.1:p.Val1599=
|
|
NM_198578.4:c.6000G>T
MANE Select
|
NP_940980.4:p.Val2000=
|
|