ENST00000298910.12:c.6519C>G
MANE Select
|
ENSP00000298910.7:p.His2173Gln
|
|
ENST00000636518.1:c.316C>G
|
|
|
ENST00000679360.1:c.*5428C>G
|
ENSP00000505368.1:n.*5428C>G
|
|
ENST00000679532.1:c.2293C>G
|
|
|
ENST00000679683.1:c.309C>G
|
|
|
ENST00000680018.1:c.1964C>G
|
ENSP00000505347.1:n.1964C>G
|
|
ENST00000680422.1:c.2164C>G
|
|
|
ENST00000680425.1:c.1686C>G
|
ENSP00000506459.1:n.1686C>G
|
|
ENST00000680453.1:c.1976C>G
|
|
|
ENST00000680790.1:c.6264C>G
|
ENSP00000505335.1:p.His2088Gln
|
|
ENST00000681136.1:n.2503C>G
|
|
|
ENST00000681696.1:c.2202C>G
|
ENSP00000505871.1:p.His734Gln
|
|
ENST00000298910.11:c.6519C>G
|
ENSP00000298910.7:p.His2173Gln
|
|
ENST00000430804.5:c.3815C>G
|
|
|
ENST00000479187.5:n.3200C>G
|
|
|
NM_198578.3:c.6519C>G
|
NP_940980.3:p.His2173Gln
|
|
XM_005268629.2:c.6519C>G
|
XP_005268686.1:p.His2173Gln
|
|
XM_011537877.1:c.6519C>G
|
XP_011536179.1:p.His2173Gln
|
|
XM_011537878.1:c.6519C>G
|
XP_011536180.1:p.His2173Gln
|
|
XM_011537879.1:c.5316C>G
|
XP_011536181.1:p.His1772Gln
|
|
XM_005268629.4:c.6519C>G
|
XP_005268686.1:p.His2173Gln
|
|
XM_011537877.3:c.6519C>G
|
XP_011536179.1:p.His2173Gln
|
|
XM_017018787.1:c.3435C>G
|
XP_016874276.1:p.His1145Gln
|
|
XM_017018788.2:c.2781C>G
|
XP_016874277.1:p.His927Gln
|
|
XM_024448833.1:c.5316C>G
|
XP_024304601.1:p.His1772Gln
|
|
NM_198578.4:c.6519C>G
MANE Select
|
NP_940980.4:p.His2173Gln
|
|