ENST00000370360.8:c.1192C>G
MANE Select
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ENSP00000359385.3:p.Gln398Glu
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ENST00000370360.7:c.1192C>G
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ENSP00000359385.3:p.Gln398Glu
|
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ENST00000463560.1:c.562+99C>G
|
|
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ENST00000495106.5:c.1192C>G
|
ENSP00000436829.1:p.Gln398Glu
|
|
ENST00000495852.6:c.415C>G
|
ENSP00000469157.2:p.Gln139Glu
|
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NM_053274.2:c.1192C>G
|
NP_444504.1:p.Gln398Glu
|
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XM_005270400.1:c.1150C>G
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XP_005270457.1:p.Gln384Glu
|
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XM_005270401.2:c.1066C>G
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XP_005270458.1:p.Gln356Glu
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XM_006710309.1:c.691C>G
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XP_006710372.1:p.Gln231Glu
|
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XM_011540544.1:c.1192C>G
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XP_011538846.1:p.Gln398Glu
|
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XM_011540545.1:c.1192C>G
|
XP_011538847.1:p.Gln398Glu
|
|
XM_011540546.1:c.1192C>G
|
XP_011538848.1:p.Gln398Glu
|
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XR_946529.1:n.1309+99C>G
|
|
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NM_001319683.1:c.1150C>G
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NP_001306612.1:p.Gln384Glu
|
|
NR_135089.1:n.1307C>G
|
|
|
XM_005270401.3:c.1066C>G
|
XP_005270458.1:p.Gln356Glu
|
|
XM_006710309.2:c.691C>G
|
XP_006710372.1:p.Gln231Glu
|
|
XM_011540546.2:c.1192C>G
|
XP_011538848.1:p.Gln398Glu
|
|
XM_017000137.1:c.1291C>G
|
XP_016855626.1:p.Gln431Glu
|
|
XM_017000138.1:c.1249C>G
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XP_016855627.1:p.Gln417Glu
|
|
XM_017000139.1:c.1293+99C>G
|
XP_016855628.1:n.1293+99C>G
|
|
XM_017000140.1:c.1165C>G
|
XP_016855629.1:p.Gln389Glu
|
|
XM_017000141.1:c.1194+99C>G
|
XP_016855630.1:n.1194+99C>G
|
|
XM_017000142.1:c.649C>G
|
XP_016855631.1:p.Gln217Glu
|
|
XM_017000143.1:c.649C>G
|
XP_016855632.1:p.Gln217Glu
|
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XM_017000144.1:c.421C>G
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XP_016855633.1:p.Gln141Glu
|
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XR_002959248.1:n.1677+99C>G
|
|
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XR_002959249.1:n.1309+99C>G
|
|
|
NM_053274.3:c.1192C>G
MANE Select
|
NP_444504.1:p.Gln398Glu
|
|
NM_001319683.2:c.1150C>G
|
NP_001306612.1:p.Gln384Glu
|
|
NR_135089.2:n.1285C>G
|
|
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