ENST00000320185.7:c.413G>C
MANE Select
|
ENSP00000321797.2:p.Cys138Ser
|
|
ENST00000618991.5:c.101G>C
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ENSP00000484420.1:p.Cys34Ser
|
|
ENST00000344255.8:c.380G>C
|
ENSP00000340039.3:p.Cys127Ser
|
|
ENST00000320185.6:c.413G>C
|
ENSP00000321797.2:p.Cys138Ser
|
|
ENST00000344255.7:c.380G>C
|
ENSP00000340039.3:p.Cys127Ser
|
|
ENST00000346714.7:c.293G>C
|
ENSP00000344306.3:p.Cys98Ser
|
|
ENST00000347978.2:c.326G>C
|
ENSP00000321945.2:p.Cys109Ser
|
|
ENST00000469792.6:c.*377G>C
|
ENSP00000473299.1:n.*377G>C
|
|
ENST00000485728.1:n.289G>C
|
|
|
ENST00000618991.4:c.101G>C
|
ENSP00000484420.1:p.Cys34Ser
|
|
NM_001206389.1:c.101G>C
|
NP_001193318.1:p.Cys34Ser
|
|
NM_006119.4:c.326G>C
|
NP_006110.1:p.Cys109Ser
|
|
NM_033163.3:c.413G>C
|
NP_149353.1:p.Cys138Ser
|
|
NM_033164.3:c.380G>C
|
NP_149354.1:p.Cys127Ser
|
|
NM_033165.3:c.293G>C
|
NP_149355.1:p.Cys98Ser
|
|
XM_011539509.1:c.335G>C
|
XP_011537811.1:p.Cys112Ser
|
|
XR_946251.1:n.278-3C>G
|
|
|
XR_946252.1:n.209-3C>G
|
|
|
XR_946253.1:n.207-3C>G
|
|
|
XR_946252.2:n.299-3C>G
|
|
|
XR_946253.2:n.297-3C>G
|
|
|
NM_006119.5:c.326G>C
|
NP_006110.1:p.Cys109Ser
|
|
NM_033163.4:c.413G>C
|
NP_149353.1:p.Cys138Ser
|
|
NM_033164.4:c.380G>C
|
NP_149354.1:p.Cys127Ser
|
|
NM_033165.4:c.293G>C
|
NP_149355.1:p.Cys98Ser
|
|
NM_001206389.2:c.101G>C
|
NP_001193318.1:p.Cys34Ser
|
|
NM_006119.6:c.326G>C
|
NP_006110.1:p.Cys109Ser
|
|
NM_033163.5:c.413G>C
MANE Select
|
NP_149353.1:p.Cys138Ser
|
|
NM_033165.5:c.293G>C
|
NP_149355.1:p.Cys98Ser
|
|