ENST00000298910.12:c.6033C>T
MANE Select
|
ENSP00000298910.7:p.Ile2011=
|
|
ENST00000679360.1:c.*4942C>T
|
ENSP00000505368.1:n.*4942C>T
|
|
ENST00000679532.1:c.1807C>T
|
|
|
ENST00000680018.1:c.1478C>T
|
ENSP00000505347.1:n.1478C>T
|
|
ENST00000680422.1:c.1678C>T
|
|
|
ENST00000680425.1:c.1200C>T
|
ENSP00000506459.1:n.1200C>T
|
|
ENST00000680453.1:c.1490C>T
|
|
|
ENST00000680790.1:c.5778C>T
|
ENSP00000505335.1:p.Ile1926=
|
|
ENST00000681136.1:n.2017C>T
|
|
|
ENST00000681696.1:c.1716C>T
|
ENSP00000505871.1:p.Ile572=
|
|
ENST00000298910.11:c.6033C>T
|
ENSP00000298910.7:p.Ile2011=
|
|
ENST00000430804.5:c.3329C>T
|
|
|
ENST00000479187.5:n.2714C>T
|
|
|
NM_198578.3:c.6033C>T
|
NP_940980.3:p.Ile2011=
|
|
XM_005268629.2:c.6033C>T
|
XP_005268686.1:p.Ile2011=
|
|
XM_011537877.1:c.6033C>T
|
XP_011536179.1:p.Ile2011=
|
|
XM_011537878.1:c.6033C>T
|
XP_011536180.1:p.Ile2011=
|
|
XM_011537879.1:c.4830C>T
|
XP_011536181.1:p.Ile1610=
|
|
XM_005268629.4:c.6033C>T
|
XP_005268686.1:p.Ile2011=
|
|
XM_011537877.3:c.6033C>T
|
XP_011536179.1:p.Ile2011=
|
|
XM_017018787.1:c.2949C>T
|
XP_016874276.1:p.Ile983=
|
|
XM_017018788.2:c.2295C>T
|
XP_016874277.1:p.Ile765=
|
|
XM_024448833.1:c.4830C>T
|
XP_024304601.1:p.Ile1610=
|
|
NM_198578.4:c.6033C>T
MANE Select
|
NP_940980.4:p.Ile2011=
|
|