ENST00000356141.9:c.1747T>G
MANE Select
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ENSP00000348460.4:p.Ser583Ala
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ENST00000551634.6:c.1756T>G
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ENSP00000448373.2:p.Ser586Ala
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ENST00000680362.1:c.1647T>G
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ENST00000681323.1:c.793+2473T>G
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ENST00000346562.6:c.1651T>G
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ENSP00000319610.5:p.Ser551Ala
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ENST00000356141.8:c.1747T>G
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ENSP00000348460.4:p.Ser583Ala
|
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ENST00000357798.9:c.1708T>G
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ENSP00000350446.5:p.Ser570Ala
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ENST00000548645.5:c.1657T>G
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ENSP00000448916.1:p.Ser553Ala
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ENST00000551492.5:c.1762T>G
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ENSP00000450392.1:p.Ser588Ala
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ENST00000551634.5:c.1669T>G
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ENSP00000448373.1:p.Ser557Ala
|
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NM_001164749.1:c.1747T>G
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NP_001158221.1:p.Ser583Ala
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NM_001165893.1:c.1657T>G
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NP_001159365.1:p.Ser553Ala
|
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NM_022123.2:c.1651T>G
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NP_071406.1:p.Ser551Ala
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NM_173159.2:c.1708T>G
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NP_775182.1:p.Ser570Ala
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XM_005267991.2:c.1768T>G
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XP_005268048.1:p.Ser590Ala
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XM_005267992.2:c.1762T>G
|
XP_005268049.1:p.Ser588Ala
|
|
XM_005267993.2:c.1708T>G
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XP_005268050.1:p.Ser570Ala
|
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XM_011537067.1:c.1798T>G
|
XP_011535369.1:p.Ser600Ala
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|
XM_011537068.1:c.1789T>G
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XP_011535370.1:p.Ser597Ala
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XM_011537069.1:c.1759T>G
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XP_011535371.1:p.Ser587Ala
|
|
XM_011537070.1:c.1702T>G
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XP_011535372.1:p.Ser568Ala
|
|
XM_011537071.1:c.1669T>G
|
XP_011535373.1:p.Ser557Ala
|
|
XM_011537072.1:c.1648T>G
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XP_011535374.1:p.Ser550Ala
|
|
XM_011537073.1:c.1441T>G
|
XP_011535375.1:p.Ser481Ala
|
|
XM_011537074.1:c.1441T>G
|
XP_011535376.1:p.Ser481Ala
|
|
XM_005267991.3:c.1855T>G
|
XP_005268048.2:p.Ser619Ala
|
|
XM_005267992.3:c.1849T>G
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XP_005268049.2:p.Ser617Ala
|
|
XM_011537067.2:c.1798T>G
|
XP_011535369.1:p.Ser600Ala
|
|
XM_011537069.2:c.1846T>G
|
XP_011535371.2:p.Ser616Ala
|
|
XM_011537070.2:c.1702T>G
|
XP_011535372.1:p.Ser568Ala
|
|
XM_011537071.2:c.1756T>G
|
XP_011535373.2:p.Ser586Ala
|
|
XM_011537072.2:c.1648T>G
|
XP_011535374.1:p.Ser550Ala
|
|
XM_017021582.1:c.1906T>G
|
XP_016877071.1:p.Ser636Ala
|
|
XM_017021583.1:c.1897T>G
|
XP_016877072.1:p.Ser633Ala
|
|
XM_017021584.1:c.1816T>G
|
XP_016877073.1:p.Ser606Ala
|
|
XM_017021585.1:c.1765T>G
|
XP_016877074.1:p.Ser589Ala
|
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XM_017021586.1:c.1441T>G
|
XP_016877075.1:p.Ser481Ala
|
|
XM_017021587.1:c.1441T>G
|
XP_016877076.1:p.Ser481Ala
|
|
XM_017021588.1:c.1441T>G
|
XP_016877077.1:p.Ser481Ala
|
|
NM_001164749.2:c.1747T>G
MANE Select
|
NP_001158221.1:p.Ser583Ala
|
|
NM_001165893.2:c.1657T>G
|
NP_001159365.1:p.Ser553Ala
|
|
NM_022123.3:c.1651T>G
|
NP_071406.1:p.Ser551Ala
|
|
NM_173159.3:c.1708T>G
|
NP_775182.1:p.Ser570Ala
|
|
NM_001394988.1:c.1702T>G
|
NP_001381917.1:p.Ser568Ala
|
|
NM_001394989.1:c.1648T>G
|
NP_001381918.1:p.Ser550Ala
|
|