ENST00000264228.9:c.302G>T
MANE Select
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ENSP00000264228.4:p.Gly101Val
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ENST00000677177.2:c.15G>T
|
|
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ENST00000678717.1:n.199G>T
|
|
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ENST00000679351.1:c.302G>T
|
ENSP00000505676.1:p.Gly101Val
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ENST00000679707.1:c.302G>T
|
ENSP00000505713.1:p.Gly101Val
|
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ENST00000679836.1:c.302G>T
|
ENSP00000506601.1:p.Gly101Val
|
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ENST00000680700.1:c.302G>T
|
ENSP00000504926.1:p.Gly101Val
|
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ENST00000264228.8:c.302G>T
|
ENSP00000264228.4:p.Gly101Val
|
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ENST00000505210.1:c.227G>T
|
ENSP00000424714.1:p.Gly76Val
|
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ENST00000514398.1:n.311G>T
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NM_024592.4:c.302G>T
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NP_078868.1:p.Gly101Val
|
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XM_005265766.2:c.302G>T
|
XP_005265823.1:p.Gly101Val
|
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XM_005265767.2:c.302G>T
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XP_005265824.1:p.Gly101Val
|
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XM_005265766.4:c.302G>T
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XP_005265823.1:p.Gly101Val
|
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XM_005265767.3:c.302G>T
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XP_005265824.1:p.Gly101Val
|
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XM_017008601.1:c.167G>T
|
XP_016864090.1:p.Gly56Val
|
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NM_024592.5:c.302G>T
MANE Select
|
NP_078868.1:p.Gly101Val
|
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