ENST00000399503.4:c.2561G>A
MANE Select
|
ENSP00000382423.3:p.Arg854His
|
|
ENST00000399503.3:c.2561G>A
|
ENSP00000382423.3:p.Arg854His
|
|
NM_005921.1:c.2561G>A
|
NP_005912.1:p.Arg854His
|
|
XM_005248519.3:c.2183G>A
|
XP_005248576.2:p.Arg728His
|
|
XM_011543406.1:c.2306G>A
|
XP_011541708.1:p.Arg769His
|
|
XM_011543407.1:c.2282G>A
|
XP_011541709.1:p.Arg761His
|
|
XM_011543408.1:c.2561G>A
|
XP_011541710.1:p.Arg854His
|
|
XM_017009484.1:c.2150G>A
|
XP_016864973.1:p.Arg717His
|
|
XM_017009485.1:c.2072G>A
|
XP_016864974.1:p.Arg691His
|
|
XR_001742068.2:n.2592G>A
|
|
|
NM_005921.2:c.2561G>A
MANE Select
|
NP_005912.1:p.Arg854His
|
|