ENST00000399503.4:c.3047C>G
MANE Select
|
ENSP00000382423.3:p.Ser1016Cys
|
|
ENST00000399503.3:c.3047C>G
|
ENSP00000382423.3:p.Ser1016Cys
|
|
NM_005921.1:c.3047C>G
|
NP_005912.1:p.Ser1016Cys
|
|
XM_005248519.3:c.2669C>G
|
XP_005248576.2:p.Ser890Cys
|
|
XM_011543406.1:c.2792C>G
|
XP_011541708.1:p.Ser931Cys
|
|
XM_011543407.1:c.2768C>G
|
XP_011541709.1:p.Ser923Cys
|
|
XM_011543408.1:c.3047C>G
|
XP_011541710.1:p.Ser1016Cys
|
|
XM_017009484.1:c.2636C>G
|
XP_016864973.1:p.Ser879Cys
|
|
XM_017009485.1:c.2558C>G
|
XP_016864974.1:p.Ser853Cys
|
|
XR_001742068.2:n.3078C>G
|
|
|
NM_005921.2:c.3047C>G
MANE Select
|
NP_005912.1:p.Ser1016Cys
|
|