ENST00000298910.12:c.7063A>G
MANE Select
|
ENSP00000298910.7:p.Ile2355Val
|
|
ENST00000636518.1:c.860A>G
|
|
|
ENST00000679360.1:c.*5972A>G
|
ENSP00000505368.1:n.*5972A>G
|
|
ENST00000679532.1:c.2837A>G
|
|
|
ENST00000679683.1:c.853A>G
|
|
|
ENST00000680018.1:c.2508A>G
|
ENSP00000505347.1:n.2508A>G
|
|
ENST00000680422.1:c.4150A>G
|
|
|
ENST00000680425.1:c.2230A>G
|
ENSP00000506459.1:n.2230A>G
|
|
ENST00000680453.1:c.2520A>G
|
|
|
ENST00000680790.1:c.6808A>G
|
ENSP00000505335.1:p.Ile2270Val
|
|
ENST00000681136.1:n.3047A>G
|
|
|
ENST00000681696.1:c.2746A>G
|
ENSP00000505871.1:p.Ile916Val
|
|
ENST00000681773.1:n.270A>G
|
|
|
ENST00000298910.11:c.7063A>G
|
ENSP00000298910.7:p.Ile2355Val
|
|
ENST00000430804.5:c.4359A>G
|
|
|
ENST00000479187.5:n.3744A>G
|
|
|
NM_198578.3:c.7063A>G
|
NP_940980.3:p.Ile2355Val
|
|
XM_005268629.2:c.7063A>G
|
XP_005268686.1:p.Ile2355Val
|
|
XM_011537877.1:c.7063A>G
|
XP_011536179.1:p.Ile2355Val
|
|
XM_011537879.1:c.5860A>G
|
XP_011536181.1:p.Ile1954Val
|
|
XR_944868.1:n.485-8609T>C
|
|
|
XM_005268629.4:c.7063A>G
|
XP_005268686.1:p.Ile2355Val
|
|
XM_011537877.3:c.7063A>G
|
XP_011536179.1:p.Ile2355Val
|
|
XM_017018787.1:c.3979A>G
|
XP_016874276.1:p.Ile1327Val
|
|
XM_017018788.2:c.3325A>G
|
XP_016874277.1:p.Ile1109Val
|
|
XM_024448833.1:c.5860A>G
|
XP_024304601.1:p.Ile1954Val
|
|
XR_944868.2:n.485-8609T>C
|
|
|
NM_198578.4:c.7063A>G
MANE Select
|
NP_940980.4:p.Ile2355Val
|
|