ENST00000298910.12:c.7177T>C
MANE Select
|
ENSP00000298910.7:p.Leu2393=
|
|
ENST00000636518.1:c.974T>C
|
|
|
ENST00000679360.1:c.*6086T>C
|
ENSP00000505368.1:n.*6086T>C
|
|
ENST00000679532.1:c.2951T>C
|
|
|
ENST00000679683.1:c.967T>C
|
|
|
ENST00000680018.1:c.2622T>C
|
ENSP00000505347.1:n.2622T>C
|
|
ENST00000680422.1:c.4264T>C
|
|
|
ENST00000680425.1:c.2344T>C
|
ENSP00000506459.1:n.2344T>C
|
|
ENST00000680453.1:c.2634T>C
|
|
|
ENST00000680790.1:c.6922T>C
|
ENSP00000505335.1:p.Leu2308=
|
|
ENST00000681136.1:n.3161T>C
|
|
|
ENST00000681696.1:c.2860T>C
|
ENSP00000505871.1:p.Leu954=
|
|
ENST00000681773.1:n.384T>C
|
|
|
ENST00000298910.11:c.7177T>C
|
ENSP00000298910.7:p.Leu2393=
|
|
ENST00000430804.5:c.4473T>C
|
|
|
ENST00000479187.5:n.3858T>C
|
|
|
NM_198578.3:c.7177T>C
|
NP_940980.3:p.Leu2393=
|
|
XM_005268629.2:c.7177T>C
|
XP_005268686.1:p.Leu2393=
|
|
XM_011537877.1:c.7177T>C
|
XP_011536179.1:p.Leu2393=
|
|
XM_011537879.1:c.5974T>C
|
XP_011536181.1:p.Leu1992=
|
|
XR_944868.1:n.485-8723A>G
|
|
|
XM_005268629.4:c.7177T>C
|
XP_005268686.1:p.Leu2393=
|
|
XM_011537877.3:c.7177T>C
|
XP_011536179.1:p.Leu2393=
|
|
XM_017018787.1:c.4093T>C
|
XP_016874276.1:p.Leu1365=
|
|
XM_017018788.2:c.3439T>C
|
XP_016874277.1:p.Leu1147=
|
|
XM_024448833.1:c.5974T>C
|
XP_024304601.1:p.Leu1992=
|
|
XR_944868.2:n.485-8723A>G
|
|
|
NM_198578.4:c.7177T>C
MANE Select
|
NP_940980.4:p.Leu2393=
|
|