ENST00000399503.4:c.812G>T
MANE Select
|
ENSP00000382423.3:p.Arg271Ile
|
|
ENST00000399503.3:c.812G>T
|
ENSP00000382423.3:p.Arg271Ile
|
|
NM_005921.1:c.812G>T
|
NP_005912.1:p.Arg271Ile
|
|
XM_005248519.3:c.434G>T
|
XP_005248576.2:p.Arg145Ile
|
|
XM_011543406.1:c.557G>T
|
XP_011541708.1:p.Arg186Ile
|
|
XM_011543407.1:c.812G>T
|
XP_011541709.1:p.Arg271Ile
|
|
XM_011543408.1:c.812G>T
|
XP_011541710.1:p.Arg271Ile
|
|
XM_017009484.1:c.401G>T
|
XP_016864973.1:p.Arg134Ile
|
|
XM_017009485.1:c.323G>T
|
XP_016864974.1:p.Arg108Ile
|
|
XR_001742068.2:n.843G>T
|
|
|
NM_005921.2:c.812G>T
MANE Select
|
NP_005912.1:p.Arg271Ile
|
|