ENST00000356231.4:c.1770T>G
MANE Select
|
ENSP00000348564.3:p.Ser590Arg
|
|
ENST00000643434.1:c.*948T>G
|
ENSP00000494699.1:n.*948T>G
|
|
ENST00000356231.3:c.1770T>G
|
ENSP00000348564.3:p.Ser590Arg
|
|
NM_138477.2:c.1770T>G
|
NP_612486.2:p.Ser590Arg
|
|
XM_005254176.3:c.1773T>G
|
XP_005254233.1:p.Ser591Arg
|
|
XM_011521270.1:c.1797T>G
|
XP_011519572.1:p.Ser599Arg
|
|
XM_011521271.1:c.1794T>G
|
XP_011519573.1:p.Ser598Arg
|
|
XM_011521272.1:c.1797T>G
|
XP_011519574.1:p.Ser599Arg
|
|
XM_011521273.1:c.1797T>G
|
XP_011519575.1:p.Ser599Arg
|
|
XM_011521274.1:c.762T>G
|
XP_011519576.1:p.Ser254Arg
|
|
XM_011521275.1:c.1014T>G
|
XP_011519577.1:p.Ser338Arg
|
|
XR_931757.1:n.1808T>G
|
|
|
NM_138477.4:c.1770T>G
MANE Select
|
NP_612486.2:p.Ser590Arg
|
|
XM_005254176.5:c.1773T>G
|
XP_005254233.1:p.Ser591Arg
|
|
XM_011521270.2:c.1797T>G
|
XP_011519572.1:p.Ser599Arg
|
|
XM_011521271.2:c.1794T>G
|
XP_011519573.1:p.Ser598Arg
|
|
XM_011521274.2:c.762T>G
|
XP_011519576.1:p.Ser254Arg
|
|
XR_001751104.1:n.1827T>G
|
|
|
XR_001751105.1:n.1827T>G
|
|
|
XR_931757.2:n.1828T>G
|
|
|