ENST00000399503.4:c.679C>G
MANE Select
|
ENSP00000382423.3:p.His227Asp
|
|
ENST00000399503.3:c.679C>G
|
ENSP00000382423.3:p.His227Asp
|
|
NM_005921.1:c.679C>G
|
NP_005912.1:p.His227Asp
|
|
XM_005248519.3:c.301C>G
|
XP_005248576.2:p.His101Asp
|
|
XM_011543406.1:c.424C>G
|
XP_011541708.1:p.His142Asp
|
|
XM_011543407.1:c.679C>G
|
XP_011541709.1:p.His227Asp
|
|
XM_011543408.1:c.679C>G
|
XP_011541710.1:p.His227Asp
|
|
XM_017009484.1:c.268C>G
|
XP_016864973.1:p.His90Asp
|
|
XM_017009485.1:c.190C>G
|
XP_016864974.1:p.His64Asp
|
|
XR_001742068.2:n.710C>G
|
|
|
NM_005921.2:c.679C>G
MANE Select
|
NP_005912.1:p.His227Asp
|
|