ENST00000399503.4:c.2966C>G
MANE Select
|
ENSP00000382423.3:p.Ser989Cys
|
|
ENST00000399503.3:c.2966C>G
|
ENSP00000382423.3:p.Ser989Cys
|
|
NM_005921.1:c.2966C>G
|
NP_005912.1:p.Ser989Cys
|
|
XM_005248519.3:c.2588C>G
|
XP_005248576.2:p.Ser863Cys
|
|
XM_011543406.1:c.2711C>G
|
XP_011541708.1:p.Ser904Cys
|
|
XM_011543407.1:c.2687C>G
|
XP_011541709.1:p.Ser896Cys
|
|
XM_011543408.1:c.2966C>G
|
XP_011541710.1:p.Ser989Cys
|
|
XM_017009484.1:c.2555C>G
|
XP_016864973.1:p.Ser852Cys
|
|
XM_017009485.1:c.2477C>G
|
XP_016864974.1:p.Ser826Cys
|
|
XR_001742068.2:n.2997C>G
|
|
|
NM_005921.2:c.2966C>G
MANE Select
|
NP_005912.1:p.Ser989Cys
|
|