ENST00000356141.9:c.1892T>G
MANE Select
|
ENSP00000348460.4:p.Val631Gly
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ENST00000551634.6:c.1901T>G
|
ENSP00000448373.2:p.Val634Gly
|
|
ENST00000680362.1:c.1792T>G
|
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ENST00000681323.1:c.793+2618T>G
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ENST00000346562.6:c.1796T>G
|
ENSP00000319610.5:p.Val599Gly
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ENST00000356141.8:c.1892T>G
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ENSP00000348460.4:p.Val631Gly
|
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ENST00000357798.9:c.1853T>G
|
ENSP00000350446.5:p.Val618Gly
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ENST00000548645.5:c.1802T>G
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ENSP00000448916.1:p.Val601Gly
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ENST00000551492.5:c.1907T>G
|
ENSP00000450392.1:p.Val636Gly
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ENST00000551634.5:c.1814T>G
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ENSP00000448373.1:p.Val605Gly
|
|
NM_001164749.1:c.1892T>G
|
NP_001158221.1:p.Val631Gly
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NM_001165893.1:c.1802T>G
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NP_001159365.1:p.Val601Gly
|
|
NM_022123.2:c.1796T>G
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NP_071406.1:p.Val599Gly
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NM_173159.2:c.1853T>G
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NP_775182.1:p.Val618Gly
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|
XM_005267991.2:c.1913T>G
|
XP_005268048.1:p.Val638Gly
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XM_005267992.2:c.1907T>G
|
XP_005268049.1:p.Val636Gly
|
|
XM_005267993.2:c.1853T>G
|
XP_005268050.1:p.Val618Gly
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|
XM_011537067.1:c.1943T>G
|
XP_011535369.1:p.Val648Gly
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|
XM_011537068.1:c.1934T>G
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XP_011535370.1:p.Val645Gly
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|
XM_011537069.1:c.1904T>G
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XP_011535371.1:p.Val635Gly
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|
XM_011537070.1:c.1847T>G
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XP_011535372.1:p.Val616Gly
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|
XM_011537071.1:c.1814T>G
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XP_011535373.1:p.Val605Gly
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XM_011537072.1:c.1793T>G
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XP_011535374.1:p.Val598Gly
|
|
XM_011537073.1:c.1586T>G
|
XP_011535375.1:p.Val529Gly
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|
XM_011537074.1:c.1586T>G
|
XP_011535376.1:p.Val529Gly
|
|
XM_005267991.3:c.2000T>G
|
XP_005268048.2:p.Val667Gly
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XM_005267992.3:c.1994T>G
|
XP_005268049.2:p.Val665Gly
|
|
XM_011537067.2:c.1943T>G
|
XP_011535369.1:p.Val648Gly
|
|
XM_011537069.2:c.1991T>G
|
XP_011535371.2:p.Val664Gly
|
|
XM_011537070.2:c.1847T>G
|
XP_011535372.1:p.Val616Gly
|
|
XM_011537071.2:c.1901T>G
|
XP_011535373.2:p.Val634Gly
|
|
XM_011537072.2:c.1793T>G
|
XP_011535374.1:p.Val598Gly
|
|
XM_017021582.1:c.2051T>G
|
XP_016877071.1:p.Val684Gly
|
|
XM_017021583.1:c.2042T>G
|
XP_016877072.1:p.Val681Gly
|
|
XM_017021584.1:c.1961T>G
|
XP_016877073.1:p.Val654Gly
|
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XM_017021585.1:c.1910T>G
|
XP_016877074.1:p.Val637Gly
|
|
XM_017021586.1:c.1586T>G
|
XP_016877075.1:p.Val529Gly
|
|
XM_017021587.1:c.1586T>G
|
XP_016877076.1:p.Val529Gly
|
|
XM_017021588.1:c.1586T>G
|
XP_016877077.1:p.Val529Gly
|
|
NM_001164749.2:c.1892T>G
MANE Select
|
NP_001158221.1:p.Val631Gly
|
|
NM_001165893.2:c.1802T>G
|
NP_001159365.1:p.Val601Gly
|
|
NM_022123.3:c.1796T>G
|
NP_071406.1:p.Val599Gly
|
|
NM_173159.3:c.1853T>G
|
NP_775182.1:p.Val618Gly
|
|
NM_001394988.1:c.1847T>G
|
NP_001381917.1:p.Val616Gly
|
|
NM_001394989.1:c.1793T>G
|
NP_001381918.1:p.Val598Gly
|
|