ENST00000356141.9:c.1773G>C
MANE Select
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ENSP00000348460.4:p.Ala591=
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ENST00000551634.6:c.1782G>C
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ENSP00000448373.2:p.Ala594=
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|
ENST00000680362.1:c.1673G>C
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|
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ENST00000681323.1:c.793+2499G>C
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|
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ENST00000346562.6:c.1677G>C
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ENSP00000319610.5:p.Ala559=
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ENST00000356141.8:c.1773G>C
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ENSP00000348460.4:p.Ala591=
|
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ENST00000357798.9:c.1734G>C
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ENSP00000350446.5:p.Ala578=
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ENST00000548645.5:c.1683G>C
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ENSP00000448916.1:p.Ala561=
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ENST00000551492.5:c.1788G>C
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ENSP00000450392.1:p.Ala596=
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ENST00000551634.5:c.1695G>C
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ENSP00000448373.1:p.Ala565=
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|
NM_001164749.1:c.1773G>C
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NP_001158221.1:p.Ala591=
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|
NM_001165893.1:c.1683G>C
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NP_001159365.1:p.Ala561=
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|
NM_022123.2:c.1677G>C
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NP_071406.1:p.Ala559=
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NM_173159.2:c.1734G>C
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NP_775182.1:p.Ala578=
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|
XM_005267991.2:c.1794G>C
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XP_005268048.1:p.Ala598=
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XM_005267992.2:c.1788G>C
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XP_005268049.1:p.Ala596=
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|
XM_005267993.2:c.1734G>C
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XP_005268050.1:p.Ala578=
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|
XM_011537067.1:c.1824G>C
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XP_011535369.1:p.Ala608=
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XM_011537068.1:c.1815G>C
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XP_011535370.1:p.Ala605=
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XM_011537069.1:c.1785G>C
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XP_011535371.1:p.Ala595=
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|
XM_011537070.1:c.1728G>C
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XP_011535372.1:p.Ala576=
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|
XM_011537071.1:c.1695G>C
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XP_011535373.1:p.Ala565=
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XM_011537072.1:c.1674G>C
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XP_011535374.1:p.Ala558=
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|
XM_011537073.1:c.1467G>C
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XP_011535375.1:p.Ala489=
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|
XM_011537074.1:c.1467G>C
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XP_011535376.1:p.Ala489=
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|
XM_005267991.3:c.1881G>C
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XP_005268048.2:p.Ala627=
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|
XM_005267992.3:c.1875G>C
|
XP_005268049.2:p.Ala625=
|
|
XM_011537067.2:c.1824G>C
|
XP_011535369.1:p.Ala608=
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|
XM_011537069.2:c.1872G>C
|
XP_011535371.2:p.Ala624=
|
|
XM_011537070.2:c.1728G>C
|
XP_011535372.1:p.Ala576=
|
|
XM_011537071.2:c.1782G>C
|
XP_011535373.2:p.Ala594=
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|
XM_011537072.2:c.1674G>C
|
XP_011535374.1:p.Ala558=
|
|
XM_017021582.1:c.1932G>C
|
XP_016877071.1:p.Ala644=
|
|
XM_017021583.1:c.1923G>C
|
XP_016877072.1:p.Ala641=
|
|
XM_017021584.1:c.1842G>C
|
XP_016877073.1:p.Ala614=
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|
XM_017021585.1:c.1791G>C
|
XP_016877074.1:p.Ala597=
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|
XM_017021586.1:c.1467G>C
|
XP_016877075.1:p.Ala489=
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|
XM_017021587.1:c.1467G>C
|
XP_016877076.1:p.Ala489=
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|
XM_017021588.1:c.1467G>C
|
XP_016877077.1:p.Ala489=
|
|
NM_001164749.2:c.1773G>C
MANE Select
|
NP_001158221.1:p.Ala591=
|
|
NM_001165893.2:c.1683G>C
|
NP_001159365.1:p.Ala561=
|
|
NM_022123.3:c.1677G>C
|
NP_071406.1:p.Ala559=
|
|
NM_173159.3:c.1734G>C
|
NP_775182.1:p.Ala578=
|
|
NM_001394988.1:c.1728G>C
|
NP_001381917.1:p.Ala576=
|
|
NM_001394989.1:c.1674G>C
|
NP_001381918.1:p.Ala558=
|
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