ENST00000370096.9:c.1675G>T
MANE Select
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ENSP00000359114.3:p.Gly559Cys
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ENST00000461720.6:c.1828G>T
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ENSP00000494909.1:p.Gly610Cys
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ENST00000644186.1:c.1675G>T
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ENSP00000493821.1:p.Gly559Cys
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ENST00000645458.1:c.1675G>T
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ENSP00000494179.1:p.Gly559Cys
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ENST00000647280.1:c.1675G>T
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ENSP00000494583.1:p.Gly559Cys
|
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ENST00000353414.8:c.1558G>T
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ENSP00000302551.6:p.Gly520Cys
|
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ENST00000358392.6:c.1711G>T
|
ENSP00000351163.2:p.Gly571Cys
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ENST00000370096.7:c.1675G>T
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ENSP00000359114.3:p.Gly559Cys
|
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ENST00000461720.5:n.23G>T
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|
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ENST00000512756.5:c.1327G>T
|
ENSP00000426533.1:p.Gly443Cys
|
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ENST00000635193.1:c.993G>T
|
|
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NM_001190709.1:c.1558G>T
|
NP_001177638.1:p.Gly520Cys
|
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NM_001854.3:c.1675G>T
|
NP_001845.3:p.Gly559Cys
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NM_080629.2:c.1711G>T
|
NP_542196.2:p.Gly571Cys
|
|
NM_080630.3:c.1327G>T
|
NP_542197.3:p.Gly443Cys
|
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XM_011540719.1:c.1675G>T
|
XP_011539021.1:p.Gly559Cys
|
|
XM_011540720.1:c.-85+205G>T
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XP_011539022.1:n.-85+205G>T
|
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XM_011540721.1:c.-754G>T
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XP_011539023.1:n.-754G>T
|
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XR_946545.1:n.2073G>T
|
|
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NR_134980.1:n.1993G>T
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|
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XM_017000334.1:c.1828G>T
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XP_016855823.1:p.Gly610Cys
|
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XM_017000335.1:c.1822G>T
|
XP_016855824.1:p.Gly608Cys
|
|
XM_017000336.1:c.1828G>T
|
XP_016855825.1:p.Gly610Cys
|
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XM_017000337.1:c.226G>T
|
XP_016855826.1:p.Gly76Cys
|
|
NM_001854.4:c.1675G>T
MANE Select
|
NP_001845.3:p.Gly559Cys
|
|
NM_080630.4:c.1327G>T
|
NP_542197.3:p.Gly443Cys
|
|
NR_134980.2:n.2019G>T
|
|
|
NM_001190709.2:c.1558G>T
|
NP_001177638.1:p.Gly520Cys
|
|
NM_080629.3:c.1711G>T
|
NP_542196.2:p.Gly571Cys
|
|