ENST00000356141.9:c.1825G>T
MANE Select
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ENSP00000348460.4:p.Gly609Cys
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ENST00000551634.6:c.1834G>T
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ENSP00000448373.2:p.Gly612Cys
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ENST00000680362.1:c.1725G>T
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ENST00000681323.1:c.793+2551G>T
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ENST00000346562.6:c.1729G>T
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ENSP00000319610.5:p.Gly577Cys
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ENST00000356141.8:c.1825G>T
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ENSP00000348460.4:p.Gly609Cys
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ENST00000357798.9:c.1786G>T
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ENSP00000350446.5:p.Gly596Cys
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ENST00000548645.5:c.1735G>T
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ENSP00000448916.1:p.Gly579Cys
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ENST00000551492.5:c.1840G>T
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ENSP00000450392.1:p.Gly614Cys
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ENST00000551634.5:c.1747G>T
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ENSP00000448373.1:p.Gly583Cys
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NM_001164749.1:c.1825G>T
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NP_001158221.1:p.Gly609Cys
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NM_001165893.1:c.1735G>T
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NP_001159365.1:p.Gly579Cys
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NM_022123.2:c.1729G>T
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NP_071406.1:p.Gly577Cys
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NM_173159.2:c.1786G>T
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NP_775182.1:p.Gly596Cys
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XM_005267991.2:c.1846G>T
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XP_005268048.1:p.Gly616Cys
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XM_005267992.2:c.1840G>T
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XP_005268049.1:p.Gly614Cys
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XM_005267993.2:c.1786G>T
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XP_005268050.1:p.Gly596Cys
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XM_011537067.1:c.1876G>T
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XP_011535369.1:p.Gly626Cys
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XM_011537068.1:c.1867G>T
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XP_011535370.1:p.Gly623Cys
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XM_011537069.1:c.1837G>T
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XP_011535371.1:p.Gly613Cys
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XM_011537070.1:c.1780G>T
|
XP_011535372.1:p.Gly594Cys
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XM_011537071.1:c.1747G>T
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XP_011535373.1:p.Gly583Cys
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XM_011537072.1:c.1726G>T
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XP_011535374.1:p.Gly576Cys
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|
XM_011537073.1:c.1519G>T
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XP_011535375.1:p.Gly507Cys
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XM_011537074.1:c.1519G>T
|
XP_011535376.1:p.Gly507Cys
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XM_005267991.3:c.1933G>T
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XP_005268048.2:p.Gly645Cys
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XM_005267992.3:c.1927G>T
|
XP_005268049.2:p.Gly643Cys
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XM_011537067.2:c.1876G>T
|
XP_011535369.1:p.Gly626Cys
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|
XM_011537069.2:c.1924G>T
|
XP_011535371.2:p.Gly642Cys
|
|
XM_011537070.2:c.1780G>T
|
XP_011535372.1:p.Gly594Cys
|
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XM_011537071.2:c.1834G>T
|
XP_011535373.2:p.Gly612Cys
|
|
XM_011537072.2:c.1726G>T
|
XP_011535374.1:p.Gly576Cys
|
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XM_017021582.1:c.1984G>T
|
XP_016877071.1:p.Gly662Cys
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XM_017021583.1:c.1975G>T
|
XP_016877072.1:p.Gly659Cys
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XM_017021584.1:c.1894G>T
|
XP_016877073.1:p.Gly632Cys
|
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XM_017021585.1:c.1843G>T
|
XP_016877074.1:p.Gly615Cys
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XM_017021586.1:c.1519G>T
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XP_016877075.1:p.Gly507Cys
|
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XM_017021587.1:c.1519G>T
|
XP_016877076.1:p.Gly507Cys
|
|
XM_017021588.1:c.1519G>T
|
XP_016877077.1:p.Gly507Cys
|
|
NM_001164749.2:c.1825G>T
MANE Select
|
NP_001158221.1:p.Gly609Cys
|
|
NM_001165893.2:c.1735G>T
|
NP_001159365.1:p.Gly579Cys
|
|
NM_022123.3:c.1729G>T
|
NP_071406.1:p.Gly577Cys
|
|
NM_173159.3:c.1786G>T
|
NP_775182.1:p.Gly596Cys
|
|
NM_001394988.1:c.1780G>T
|
NP_001381917.1:p.Gly594Cys
|
|
NM_001394989.1:c.1726G>T
|
NP_001381918.1:p.Gly576Cys
|
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