ENST00000309244.9:c.227G>A
MANE Select
|
ENSP00000311930.3:p.Arg76His
|
|
ENST00000309244.8:c.227G>A
|
ENSP00000311930.3:p.Arg76His
|
|
ENST00000354232.8:c.500G>A
|
ENSP00000346173.3:p.Arg167His
|
|
ENST00000593992.1:n.250G>A
|
|
|
ENST00000596253.1:c.216+870G>A
|
ENSP00000469628.1:n.216+870G>A
|
|
ENST00000600067.1:c.*153G>A
|
ENSP00000469452.1:n.*153G>A
|
|
NM_001014763.1:c.500G>A
|
NP_001014763.1:p.Arg167His
|
|
NM_001985.2:c.227G>A
|
NP_001976.1:p.Arg76His
|
|
XM_024451418.1:c.116G>A
|
XP_024307186.1:p.Arg39His
|
|
NM_001985.3:c.227G>A
MANE Select
|
NP_001976.1:p.Arg76His
|
|