ENST00000399503.4:c.3114C>G
MANE Select
|
ENSP00000382423.3:p.Asp1038Glu
|
|
ENST00000399503.3:c.3114C>G
|
ENSP00000382423.3:p.Asp1038Glu
|
|
NM_005921.1:c.3114C>G
|
NP_005912.1:p.Asp1038Glu
|
|
XM_005248519.3:c.2736C>G
|
XP_005248576.2:p.Asp912Glu
|
|
XM_011543406.1:c.2859C>G
|
XP_011541708.1:p.Asp953Glu
|
|
XM_011543407.1:c.2835C>G
|
XP_011541709.1:p.Asp945Glu
|
|
XM_011543408.1:c.3114C>G
|
XP_011541710.1:p.Asp1038Glu
|
|
XM_017009484.1:c.2703C>G
|
XP_016864973.1:p.Asp901Glu
|
|
XM_017009485.1:c.2625C>G
|
XP_016864974.1:p.Asp875Glu
|
|
XR_001742068.2:n.3145C>G
|
|
|
NM_005921.2:c.3114C>G
MANE Select
|
NP_005912.1:p.Asp1038Glu
|
|