ENST00000356141.9:c.1759G>T
MANE Select
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ENSP00000348460.4:p.Gly587Cys
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ENST00000551634.6:c.1768G>T
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ENSP00000448373.2:p.Gly590Cys
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ENST00000680362.1:c.1659G>T
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ENST00000681323.1:c.793+2485G>T
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ENST00000346562.6:c.1663G>T
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ENSP00000319610.5:p.Gly555Cys
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ENST00000356141.8:c.1759G>T
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ENSP00000348460.4:p.Gly587Cys
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ENST00000357798.9:c.1720G>T
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ENSP00000350446.5:p.Gly574Cys
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ENST00000548645.5:c.1669G>T
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ENSP00000448916.1:p.Gly557Cys
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ENST00000551492.5:c.1774G>T
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ENSP00000450392.1:p.Gly592Cys
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ENST00000551634.5:c.1681G>T
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ENSP00000448373.1:p.Gly561Cys
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NM_001164749.1:c.1759G>T
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NP_001158221.1:p.Gly587Cys
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NM_001165893.1:c.1669G>T
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NP_001159365.1:p.Gly557Cys
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NM_022123.2:c.1663G>T
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NP_071406.1:p.Gly555Cys
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NM_173159.2:c.1720G>T
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NP_775182.1:p.Gly574Cys
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XM_005267991.2:c.1780G>T
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XP_005268048.1:p.Gly594Cys
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XM_005267992.2:c.1774G>T
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XP_005268049.1:p.Gly592Cys
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XM_005267993.2:c.1720G>T
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XP_005268050.1:p.Gly574Cys
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XM_011537067.1:c.1810G>T
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XP_011535369.1:p.Gly604Cys
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XM_011537068.1:c.1801G>T
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XP_011535370.1:p.Gly601Cys
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XM_011537069.1:c.1771G>T
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XP_011535371.1:p.Gly591Cys
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XM_011537070.1:c.1714G>T
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XP_011535372.1:p.Gly572Cys
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XM_011537071.1:c.1681G>T
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XP_011535373.1:p.Gly561Cys
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XM_011537072.1:c.1660G>T
|
XP_011535374.1:p.Gly554Cys
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XM_011537073.1:c.1453G>T
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XP_011535375.1:p.Gly485Cys
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XM_011537074.1:c.1453G>T
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XP_011535376.1:p.Gly485Cys
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XM_005267991.3:c.1867G>T
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XP_005268048.2:p.Gly623Cys
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XM_005267992.3:c.1861G>T
|
XP_005268049.2:p.Gly621Cys
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XM_011537067.2:c.1810G>T
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XP_011535369.1:p.Gly604Cys
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XM_011537069.2:c.1858G>T
|
XP_011535371.2:p.Gly620Cys
|
|
XM_011537070.2:c.1714G>T
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XP_011535372.1:p.Gly572Cys
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|
XM_011537071.2:c.1768G>T
|
XP_011535373.2:p.Gly590Cys
|
|
XM_011537072.2:c.1660G>T
|
XP_011535374.1:p.Gly554Cys
|
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XM_017021582.1:c.1918G>T
|
XP_016877071.1:p.Gly640Cys
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XM_017021583.1:c.1909G>T
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XP_016877072.1:p.Gly637Cys
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XM_017021584.1:c.1828G>T
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XP_016877073.1:p.Gly610Cys
|
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XM_017021585.1:c.1777G>T
|
XP_016877074.1:p.Gly593Cys
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XM_017021586.1:c.1453G>T
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XP_016877075.1:p.Gly485Cys
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XM_017021587.1:c.1453G>T
|
XP_016877076.1:p.Gly485Cys
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XM_017021588.1:c.1453G>T
|
XP_016877077.1:p.Gly485Cys
|
|
NM_001164749.2:c.1759G>T
MANE Select
|
NP_001158221.1:p.Gly587Cys
|
|
NM_001165893.2:c.1669G>T
|
NP_001159365.1:p.Gly557Cys
|
|
NM_022123.3:c.1663G>T
|
NP_071406.1:p.Gly555Cys
|
|
NM_173159.3:c.1720G>T
|
NP_775182.1:p.Gly574Cys
|
|
NM_001394988.1:c.1714G>T
|
NP_001381917.1:p.Gly572Cys
|
|
NM_001394989.1:c.1660G>T
|
NP_001381918.1:p.Gly554Cys
|
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