ENST00000356231.4:c.2750T>G
MANE Select
|
ENSP00000348564.3:p.Ile917Ser
|
|
ENST00000643434.1:c.*1928T>G
|
ENSP00000494699.1:n.*1928T>G
|
|
ENST00000356231.3:c.2750T>G
|
ENSP00000348564.3:p.Ile917Ser
|
|
ENST00000562465.5:c.743T>G
|
ENSP00000454246.1:p.Ile248Ser
|
|
NM_138477.2:c.2750T>G
|
NP_612486.2:p.Ile917Ser
|
|
XM_005254176.3:c.2753T>G
|
XP_005254233.1:p.Ile918Ser
|
|
XM_011521270.1:c.2777T>G
|
XP_011519572.1:p.Ile926Ser
|
|
XM_011521271.1:c.2774T>G
|
XP_011519573.1:p.Ile925Ser
|
|
XM_011521272.1:c.2777T>G
|
XP_011519574.1:p.Ile926Ser
|
|
XM_011521273.1:c.2777T>G
|
XP_011519575.1:p.Ile926Ser
|
|
XM_011521274.1:c.1742T>G
|
XP_011519576.1:p.Ile581Ser
|
|
XM_011521275.1:c.1994T>G
|
XP_011519577.1:p.Ile665Ser
|
|
NM_138477.4:c.2750T>G
MANE Select
|
NP_612486.2:p.Ile917Ser
|
|
XM_005254176.5:c.2753T>G
|
XP_005254233.1:p.Ile918Ser
|
|
XM_011521270.2:c.2777T>G
|
XP_011519572.1:p.Ile926Ser
|
|
XM_011521271.2:c.2774T>G
|
XP_011519573.1:p.Ile925Ser
|
|
XM_011521274.2:c.1742T>G
|
XP_011519576.1:p.Ile581Ser
|
|
XR_001751104.1:n.2807T>G
|
|
|
XR_001751105.1:n.2807T>G
|
|
|