ENST00000356231.4:c.1852G>C
MANE Select
|
ENSP00000348564.3:p.Asp618His
|
|
ENST00000643434.1:c.*1030G>C
|
ENSP00000494699.1:n.*1030G>C
|
|
ENST00000356231.3:c.1852G>C
|
ENSP00000348564.3:p.Asp618His
|
|
NM_138477.2:c.1852G>C
|
NP_612486.2:p.Asp618His
|
|
XM_005254176.3:c.1855G>C
|
XP_005254233.1:p.Asp619His
|
|
XM_011521270.1:c.1879G>C
|
XP_011519572.1:p.Asp627His
|
|
XM_011521271.1:c.1876G>C
|
XP_011519573.1:p.Asp626His
|
|
XM_011521272.1:c.1879G>C
|
XP_011519574.1:p.Asp627His
|
|
XM_011521273.1:c.1879G>C
|
XP_011519575.1:p.Asp627His
|
|
XM_011521274.1:c.844G>C
|
XP_011519576.1:p.Asp282His
|
|
XM_011521275.1:c.1096G>C
|
XP_011519577.1:p.Asp366His
|
|
XR_931757.1:n.1890G>C
|
|
|
NM_138477.4:c.1852G>C
MANE Select
|
NP_612486.2:p.Asp618His
|
|
XM_005254176.5:c.1855G>C
|
XP_005254233.1:p.Asp619His
|
|
XM_011521270.2:c.1879G>C
|
XP_011519572.1:p.Asp627His
|
|
XM_011521271.2:c.1876G>C
|
XP_011519573.1:p.Asp626His
|
|
XM_011521274.2:c.844G>C
|
XP_011519576.1:p.Asp282His
|
|
XR_001751104.1:n.1909G>C
|
|
|
XR_001751105.1:n.1909G>C
|
|
|
XR_931757.2:n.1910G>C
|
|
|