ENST00000680821.2:c.3880C>G
MANE Select
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ENSP00000504874.1:p.Gln1294Glu
|
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ENST00000262765.10:c.3382C>G
|
ENSP00000262765.5:p.Gln1128Glu
|
|
ENST00000636395.1:c.3880C>G
|
ENSP00000490761.1:p.Gln1294Glu
|
|
ENST00000680821.1:c.3880C>G
|
ENSP00000504874.1:p.Gln1294Glu
|
|
ENST00000262765.9:c.3382C>G
|
ENSP00000262765.5:p.Gln1128Glu
|
|
ENST00000447564.2:c.406C>G
|
ENSP00000394461.2:p.Gln136Glu
|
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ENST00000524722.1:c.*146C>G
|
ENSP00000432679.1:n.*146C>G
|
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NM_032134.2:c.3382C>G
|
NP_115510.1:p.Gln1128Glu
|
|
NR_130649.1:n.653C>G
|
|
|
XM_005257728.2:c.3880C>G
|
XP_005257785.1:p.Gln1294Glu
|
|
XM_006722136.2:c.142C>G
|
XP_006722199.1:p.Gln48Glu
|
|
XM_011525344.1:c.3160C>G
|
XP_011523646.1:p.Gln1054Glu
|
|
XM_005257728.4:c.3880C>G
|
XP_005257785.1:p.Gln1294Glu
|
|
XM_006722136.3:c.142C>G
|
XP_006722199.1:p.Gln48Glu
|
|
XM_011525344.2:c.3160C>G
|
XP_011523646.1:p.Gln1054Glu
|
|
XM_017025206.2:c.3880C>G
|
XP_016880695.1:p.Gln1294Glu
|
|
XM_017025207.2:c.3820C>G
|
XP_016880696.1:p.Gln1274Glu
|
|
XM_017025208.1:c.-87C>G
|
XP_016880697.1:n.-87C>G
|
|
NM_001388453.1:c.3880C>G
MANE Select
|
NP_001375382.1:p.Gln1294Glu
|
|
NM_032134.3:c.3880C>G
|
NP_115510.2:p.Gln1294Glu
|
|
NR_130649.2:n.1249C>G
|
|
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