ENST00000298910.12:c.7119G>T
MANE Select
|
ENSP00000298910.7:p.Val2373=
|
|
ENST00000636518.1:c.916G>T
|
|
|
ENST00000679360.1:c.*6028G>T
|
ENSP00000505368.1:n.*6028G>T
|
|
ENST00000679532.1:c.2893G>T
|
|
|
ENST00000679683.1:c.909G>T
|
|
|
ENST00000680018.1:c.2564G>T
|
ENSP00000505347.1:n.2564G>T
|
|
ENST00000680422.1:c.4206G>T
|
|
|
ENST00000680425.1:c.2286G>T
|
ENSP00000506459.1:n.2286G>T
|
|
ENST00000680453.1:c.2576G>T
|
|
|
ENST00000680790.1:c.6864G>T
|
ENSP00000505335.1:p.Val2288=
|
|
ENST00000681136.1:n.3103G>T
|
|
|
ENST00000681696.1:c.2802G>T
|
ENSP00000505871.1:p.Val934=
|
|
ENST00000681773.1:n.326G>T
|
|
|
ENST00000298910.11:c.7119G>T
|
ENSP00000298910.7:p.Val2373=
|
|
ENST00000430804.5:c.4415G>T
|
|
|
ENST00000479187.5:n.3800G>T
|
|
|
NM_198578.3:c.7119G>T
|
NP_940980.3:p.Val2373=
|
|
XM_005268629.2:c.7119G>T
|
XP_005268686.1:p.Val2373=
|
|
XM_011537877.1:c.7119G>T
|
XP_011536179.1:p.Val2373=
|
|
XM_011537879.1:c.5916G>T
|
XP_011536181.1:p.Val1972=
|
|
XR_944868.1:n.485-8665C>A
|
|
|
XM_005268629.4:c.7119G>T
|
XP_005268686.1:p.Val2373=
|
|
XM_011537877.3:c.7119G>T
|
XP_011536179.1:p.Val2373=
|
|
XM_017018787.1:c.4035G>T
|
XP_016874276.1:p.Val1345=
|
|
XM_017018788.2:c.3381G>T
|
XP_016874277.1:p.Val1127=
|
|
XM_024448833.1:c.5916G>T
|
XP_024304601.1:p.Val1972=
|
|
XR_944868.2:n.485-8665C>A
|
|
|
NM_198578.4:c.7119G>T
MANE Select
|
NP_940980.4:p.Val2373=
|
|