ENST00000298910.12:c.7162G>C
MANE Select
|
ENSP00000298910.7:p.Asp2388His
|
|
ENST00000636518.1:c.959G>C
|
|
|
ENST00000679360.1:c.*6071G>C
|
ENSP00000505368.1:n.*6071G>C
|
|
ENST00000679532.1:c.2936G>C
|
|
|
ENST00000679683.1:c.952G>C
|
|
|
ENST00000680018.1:c.2607G>C
|
ENSP00000505347.1:n.2607G>C
|
|
ENST00000680422.1:c.4249G>C
|
|
|
ENST00000680425.1:c.2329G>C
|
ENSP00000506459.1:n.2329G>C
|
|
ENST00000680453.1:c.2619G>C
|
|
|
ENST00000680790.1:c.6907G>C
|
ENSP00000505335.1:p.Asp2303His
|
|
ENST00000681136.1:n.3146G>C
|
|
|
ENST00000681696.1:c.2845G>C
|
ENSP00000505871.1:p.Asp949His
|
|
ENST00000681773.1:n.369G>C
|
|
|
ENST00000298910.11:c.7162G>C
|
ENSP00000298910.7:p.Asp2388His
|
|
ENST00000430804.5:c.4458G>C
|
|
|
ENST00000479187.5:n.3843G>C
|
|
|
NM_198578.3:c.7162G>C
|
NP_940980.3:p.Asp2388His
|
|
XM_005268629.2:c.7162G>C
|
XP_005268686.1:p.Asp2388His
|
|
XM_011537877.1:c.7162G>C
|
XP_011536179.1:p.Asp2388His
|
|
XM_011537879.1:c.5959G>C
|
XP_011536181.1:p.Asp1987His
|
|
XR_944868.1:n.485-8708C>G
|
|
|
XM_005268629.4:c.7162G>C
|
XP_005268686.1:p.Asp2388His
|
|
XM_011537877.3:c.7162G>C
|
XP_011536179.1:p.Asp2388His
|
|
XM_017018787.1:c.4078G>C
|
XP_016874276.1:p.Asp1360His
|
|
XM_017018788.2:c.3424G>C
|
XP_016874277.1:p.Asp1142His
|
|
XM_024448833.1:c.5959G>C
|
XP_024304601.1:p.Asp1987His
|
|
XR_944868.2:n.485-8708C>G
|
|
|
NM_198578.4:c.7162G>C
MANE Select
|
NP_940980.4:p.Asp2388His
|
|