ENST00000298910.12:c.5518T>G
MANE Select
|
ENSP00000298910.7:p.Leu1840Val
|
|
ENST00000679360.1:c.*4427T>G
|
ENSP00000505368.1:n.*4427T>G
|
|
ENST00000679532.1:c.1292T>G
|
|
|
ENST00000680018.1:c.963T>G
|
ENSP00000505347.1:n.963T>G
|
|
ENST00000680422.1:c.1163T>G
|
|
|
ENST00000680425.1:c.685T>G
|
ENSP00000506459.1:n.685T>G
|
|
ENST00000680453.1:c.975T>G
|
|
|
ENST00000680790.1:c.5263T>G
|
ENSP00000505335.1:p.Leu1755Val
|
|
ENST00000681136.1:n.1502T>G
|
|
|
ENST00000681696.1:c.1201T>G
|
ENSP00000505871.1:p.Leu401Val
|
|
ENST00000298910.11:c.5518T>G
|
ENSP00000298910.7:p.Leu1840Val
|
|
ENST00000430804.5:c.2814T>G
|
|
|
ENST00000479187.5:n.2199T>G
|
|
|
NM_198578.3:c.5518T>G
|
NP_940980.3:p.Leu1840Val
|
|
XM_005268629.2:c.5518T>G
|
XP_005268686.1:p.Leu1840Val
|
|
XM_011537877.1:c.5518T>G
|
XP_011536179.1:p.Leu1840Val
|
|
XM_011537878.1:c.5518T>G
|
XP_011536180.1:p.Leu1840Val
|
|
XM_011537879.1:c.4315T>G
|
XP_011536181.1:p.Leu1439Val
|
|
XM_005268629.4:c.5518T>G
|
XP_005268686.1:p.Leu1840Val
|
|
XM_011537877.3:c.5518T>G
|
XP_011536179.1:p.Leu1840Val
|
|
XM_017018787.1:c.2434T>G
|
XP_016874276.1:p.Leu812Val
|
|
XM_017018788.2:c.1780T>G
|
XP_016874277.1:p.Leu594Val
|
|
XM_024448833.1:c.4315T>G
|
XP_024304601.1:p.Leu1439Val
|
|
NM_198578.4:c.5518T>G
MANE Select
|
NP_940980.4:p.Leu1840Val
|
|