ENST00000317357.10:c.1723G>T
MANE Select
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ENSP00000318900.5:p.Gly575Cys
|
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ENST00000317357.9:c.1723G>T
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ENSP00000318900.5:p.Gly575Cys
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|
NM_018013.3:c.1723G>T
|
NP_060483.3:p.Gly575Cys
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XM_005267041.3:c.1876G>T
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XP_005267098.1:p.Gly626Cys
|
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XM_005267042.3:c.1780G>T
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XP_005267099.1:p.Gly594Cys
|
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XM_011535920.1:c.1876G>T
|
XP_011534222.1:p.Gly626Cys
|
|
XM_011535921.1:c.1762G>T
|
XP_011534223.1:p.Gly588Cys
|
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XM_011535922.1:c.1135G>T
|
XP_011534224.1:p.Gly379Cys
|
|
XM_011535923.1:c.946G>T
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XP_011534225.1:p.Gly316Cys
|
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XM_005267041.4:c.1876G>T
|
XP_005267098.1:p.Gly626Cys
|
|
XM_005267042.4:c.1780G>T
|
XP_005267099.1:p.Gly594Cys
|
|
XM_011535920.2:c.1876G>T
|
XP_011534222.1:p.Gly626Cys
|
|
XM_011535921.2:c.1762G>T
|
XP_011534223.1:p.Gly588Cys
|
|
XM_011535923.2:c.946G>T
|
XP_011534225.1:p.Gly316Cys
|
|
XM_017010991.1:c.1276G>T
|
XP_016866480.1:p.Gly426Cys
|
|
XM_017010992.1:c.1276G>T
|
XP_016866481.1:p.Gly426Cys
|
|
XM_017010993.1:c.1276G>T
|
XP_016866482.1:p.Gly426Cys
|
|
XM_017010994.1:c.1276G>T
|
XP_016866483.1:p.Gly426Cys
|
|
NM_018013.4:c.1723G>T
MANE Select
|
NP_060483.3:p.Gly575Cys
|
|