ENST00000388996.10:c.880G>C
MANE Select
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ENSP00000373648.3:p.Glu294Gln
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ENST00000521134.6:c.520G>C
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ENSP00000429799.1:p.Glu174Gln
|
|
ENST00000638588.1:c.553G>C
|
ENSP00000491940.1:p.Glu185Gln
|
|
ENST00000639358.1:c.530G>C
|
|
|
ENST00000639496.1:c.553G>C
|
ENSP00000491165.1:p.Glu185Gln
|
|
ENST00000388996.8:c.880G>C
|
ENSP00000373648.3:p.Glu294Gln
|
|
ENST00000519445.5:c.880G>C
|
ENSP00000428790.1:p.Glu294Gln
|
|
ENST00000519589.1:n.658G>C
|
|
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ENST00000521134.5:c.520G>C
|
ENSP00000429799.1:p.Glu174Gln
|
|
ENST00000621976.1:c.517G>C
|
ENSP00000482510.1:p.Glu173Gln
|
|
NM_001204824.1:c.520G>C
|
NP_001191753.1:p.Glu174Gln
|
|
NM_004519.3:c.880G>C
|
NP_004510.1:p.Glu294Gln
|
|
XM_005250914.2:c.-277G>C
|
XP_005250971.1:n.-277G>C
|
|
XM_006716555.2:c.172G>C
|
XP_006716618.1:p.Glu58Gln
|
|
XM_011517026.1:c.520G>C
|
XP_011515328.1:p.Glu174Gln
|
|
XM_005250914.3:c.-277G>C
|
XP_005250971.1:n.-277G>C
|
|
XM_006716555.3:c.172G>C
|
XP_006716618.1:p.Glu58Gln
|
|
XM_011517026.2:c.520G>C
|
XP_011515328.1:p.Glu174Gln
|
|
XM_017013400.1:c.658G>C
|
XP_016868889.1:p.Glu220Gln
|
|
NM_004519.4:c.880G>C
MANE Select
|
NP_004510.1:p.Glu294Gln
|
|
NM_001204824.2:c.520G>C
|
NP_001191753.1:p.Glu174Gln
|
|