ENST00000399503.4:c.797C>G
MANE Select
|
ENSP00000382423.3:p.Ser266Cys
|
|
ENST00000399503.3:c.797C>G
|
ENSP00000382423.3:p.Ser266Cys
|
|
NM_005921.1:c.797C>G
|
NP_005912.1:p.Ser266Cys
|
|
XM_005248519.3:c.419C>G
|
XP_005248576.2:p.Ser140Cys
|
|
XM_011543406.1:c.542C>G
|
XP_011541708.1:p.Ser181Cys
|
|
XM_011543407.1:c.797C>G
|
XP_011541709.1:p.Ser266Cys
|
|
XM_011543408.1:c.797C>G
|
XP_011541710.1:p.Ser266Cys
|
|
XM_017009484.1:c.386C>G
|
XP_016864973.1:p.Ser129Cys
|
|
XM_017009485.1:c.308C>G
|
XP_016864974.1:p.Ser103Cys
|
|
XR_001742068.2:n.828C>G
|
|
|
NM_005921.2:c.797C>G
MANE Select
|
NP_005912.1:p.Ser266Cys
|
|