ENST00000399503.4:c.646A>G
MANE Select
|
ENSP00000382423.3:p.Ile216Val
|
|
ENST00000399503.3:c.646A>G
|
ENSP00000382423.3:p.Ile216Val
|
|
NM_005921.1:c.646A>G
|
NP_005912.1:p.Ile216Val
|
|
XM_005248519.3:c.268A>G
|
XP_005248576.2:p.Ile90Val
|
|
XM_011543406.1:c.391A>G
|
XP_011541708.1:p.Ile131Val
|
|
XM_011543407.1:c.646A>G
|
XP_011541709.1:p.Ile216Val
|
|
XM_011543408.1:c.646A>G
|
XP_011541710.1:p.Ile216Val
|
|
XM_017009484.1:c.235A>G
|
XP_016864973.1:p.Ile79Val
|
|
XM_017009485.1:c.157A>G
|
XP_016864974.1:p.Ile53Val
|
|
XR_001742068.2:n.677A>G
|
|
|
NM_005921.2:c.646A>G
MANE Select
|
NP_005912.1:p.Ile216Val
|
|