ENST00000256906.5:c.677A>G
MANE Select
|
ENSP00000256906.4:p.His226Arg
|
|
ENST00000256906.4:c.677A>G
|
ENSP00000256906.4:p.His226Arg
|
|
ENST00000426880.2:c.413A>G
|
ENSP00000402526.2:p.His138Arg
|
|
NM_001143828.1:c.413A>G
|
NP_001137300.1:p.His138Arg
|
|
NM_001160166.1:c.*309A>G
|
NP_001153638.1:n.*309A>G
|
|
NM_021624.3:c.677A>G
|
NP_067637.2:p.His226Arg
|
|
XM_011526133.1:c.357+8115A>G
|
XP_011524435.1:n.357+8115A>G
|
|
NM_021624.4:c.677A>G
MANE Select
|
NP_067637.2:p.His226Arg
|
|
NM_001143828.2:c.413A>G
|
NP_001137300.1:p.His138Arg
|
|
NM_001160166.2:c.*309A>G
|
NP_001153638.1:n.*309A>G
|
|