ENST00000356141.9:c.1777G>A
MANE Select
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ENSP00000348460.4:p.Ala593Thr
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ENST00000551634.6:c.1786G>A
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ENSP00000448373.2:p.Ala596Thr
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ENST00000680362.1:c.1677G>A
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ENST00000681323.1:c.793+2503G>A
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ENST00000346562.6:c.1681G>A
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ENSP00000319610.5:p.Ala561Thr
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ENST00000356141.8:c.1777G>A
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ENSP00000348460.4:p.Ala593Thr
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ENST00000357798.9:c.1738G>A
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ENSP00000350446.5:p.Ala580Thr
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ENST00000548645.5:c.1687G>A
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ENSP00000448916.1:p.Ala563Thr
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ENST00000551492.5:c.1792G>A
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ENSP00000450392.1:p.Ala598Thr
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ENST00000551634.5:c.1699G>A
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ENSP00000448373.1:p.Ala567Thr
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NM_001164749.1:c.1777G>A
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NP_001158221.1:p.Ala593Thr
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NM_001165893.1:c.1687G>A
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NP_001159365.1:p.Ala563Thr
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NM_022123.2:c.1681G>A
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NP_071406.1:p.Ala561Thr
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NM_173159.2:c.1738G>A
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NP_775182.1:p.Ala580Thr
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XM_005267991.2:c.1798G>A
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XP_005268048.1:p.Ala600Thr
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XM_005267992.2:c.1792G>A
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XP_005268049.1:p.Ala598Thr
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XM_005267993.2:c.1738G>A
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XP_005268050.1:p.Ala580Thr
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XM_011537067.1:c.1828G>A
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XP_011535369.1:p.Ala610Thr
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XM_011537068.1:c.1819G>A
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XP_011535370.1:p.Ala607Thr
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XM_011537069.1:c.1789G>A
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XP_011535371.1:p.Ala597Thr
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XM_011537070.1:c.1732G>A
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XP_011535372.1:p.Ala578Thr
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XM_011537071.1:c.1699G>A
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XP_011535373.1:p.Ala567Thr
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XM_011537072.1:c.1678G>A
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XP_011535374.1:p.Ala560Thr
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XM_011537073.1:c.1471G>A
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XP_011535375.1:p.Ala491Thr
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XM_011537074.1:c.1471G>A
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XP_011535376.1:p.Ala491Thr
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XM_005267991.3:c.1885G>A
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XP_005268048.2:p.Ala629Thr
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XM_005267992.3:c.1879G>A
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XP_005268049.2:p.Ala627Thr
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XM_011537067.2:c.1828G>A
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XP_011535369.1:p.Ala610Thr
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XM_011537069.2:c.1876G>A
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XP_011535371.2:p.Ala626Thr
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XM_011537070.2:c.1732G>A
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XP_011535372.1:p.Ala578Thr
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XM_011537071.2:c.1786G>A
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XP_011535373.2:p.Ala596Thr
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XM_011537072.2:c.1678G>A
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XP_011535374.1:p.Ala560Thr
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XM_017021582.1:c.1936G>A
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XP_016877071.1:p.Ala646Thr
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XM_017021583.1:c.1927G>A
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XP_016877072.1:p.Ala643Thr
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XM_017021584.1:c.1846G>A
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XP_016877073.1:p.Ala616Thr
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XM_017021585.1:c.1795G>A
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XP_016877074.1:p.Ala599Thr
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XM_017021586.1:c.1471G>A
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XP_016877075.1:p.Ala491Thr
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XM_017021587.1:c.1471G>A
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XP_016877076.1:p.Ala491Thr
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XM_017021588.1:c.1471G>A
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XP_016877077.1:p.Ala491Thr
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NM_001164749.2:c.1777G>A
MANE Select
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NP_001158221.1:p.Ala593Thr
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NM_001165893.2:c.1687G>A
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NP_001159365.1:p.Ala563Thr
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NM_022123.3:c.1681G>A
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NP_071406.1:p.Ala561Thr
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NM_173159.3:c.1738G>A
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NP_775182.1:p.Ala580Thr
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NM_001394988.1:c.1732G>A
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NP_001381917.1:p.Ala578Thr
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NM_001394989.1:c.1678G>A
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NP_001381918.1:p.Ala560Thr
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