ENST00000317357.10:c.1703G>T
MANE Select
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ENSP00000318900.5:p.Gly568Val
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ENST00000317357.9:c.1703G>T
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ENSP00000318900.5:p.Gly568Val
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|
NM_018013.3:c.1703G>T
|
NP_060483.3:p.Gly568Val
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XM_005267041.3:c.1856G>T
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XP_005267098.1:p.Gly619Val
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XM_005267042.3:c.1760G>T
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XP_005267099.1:p.Gly587Val
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XM_011535920.1:c.1856G>T
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XP_011534222.1:p.Gly619Val
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XM_011535921.1:c.1742G>T
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XP_011534223.1:p.Gly581Val
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XM_011535922.1:c.1115G>T
|
XP_011534224.1:p.Gly372Val
|
|
XM_011535923.1:c.926G>T
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XP_011534225.1:p.Gly309Val
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XM_005267041.4:c.1856G>T
|
XP_005267098.1:p.Gly619Val
|
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XM_005267042.4:c.1760G>T
|
XP_005267099.1:p.Gly587Val
|
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XM_011535920.2:c.1856G>T
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XP_011534222.1:p.Gly619Val
|
|
XM_011535921.2:c.1742G>T
|
XP_011534223.1:p.Gly581Val
|
|
XM_011535923.2:c.926G>T
|
XP_011534225.1:p.Gly309Val
|
|
XM_017010991.1:c.1256G>T
|
XP_016866480.1:p.Gly419Val
|
|
XM_017010992.1:c.1256G>T
|
XP_016866481.1:p.Gly419Val
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|
XM_017010993.1:c.1256G>T
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XP_016866482.1:p.Gly419Val
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XM_017010994.1:c.1256G>T
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XP_016866483.1:p.Gly419Val
|
|
NM_018013.4:c.1703G>T
MANE Select
|
NP_060483.3:p.Gly568Val
|
|