ENST00000261208.8:c.786T>C
MANE Select
|
ENSP00000261208.3:p.His262=
|
|
ENST00000261208.7:c.786T>C
|
ENSP00000261208.3:p.His262=
|
|
ENST00000538703.5:c.786T>C
|
ENSP00000440861.1:p.His262=
|
|
ENST00000541929.5:c.162T>C
|
ENSP00000446364.1:p.His54=
|
|
ENST00000544080.6:c.*215T>C
|
ENSP00000439385.2:n.*215T>C
|
|
ENST00000546999.5:c.*215T>C
|
ENSP00000447675.1:n.*215T>C
|
|
ENST00000549376.1:n.179T>C
|
|
|
ENST00000551562.1:n.46T>C
|
|
|
ENST00000552509.5:c.750T>C
|
ENSP00000450372.1:p.His250=
|
|
NM_001258333.1:c.162T>C
|
NP_001245262.1:p.His54=
|
|
NM_001258334.1:c.786T>C
|
NP_001245263.1:p.His262=
|
|
NM_002108.3:c.786T>C
|
NP_002099.1:p.His262=
|
|
XM_011538249.1:c.3+2218T>C
|
XP_011536551.1:n.3+2218T>C
|
|
XM_011538249.2:c.3+2218T>C
|
XP_011536551.1:n.3+2218T>C
|
|
NM_002108.4:c.786T>C
MANE Select
|
NP_002099.1:p.His262=
|
|
NM_001258334.2:c.786T>C
|
NP_001245263.1:p.His262=
|
|
NM_001258333.2:c.162T>C
|
NP_001245262.1:p.His54=
|
|