ENST00000356141.9:c.1740C>A
MANE Select
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ENSP00000348460.4:p.Ala580=
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ENST00000551634.6:c.1749C>A
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ENSP00000448373.2:p.Ala583=
|
|
ENST00000680362.1:c.1640C>A
|
|
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ENST00000681323.1:c.793+2466C>A
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|
|
ENST00000346562.6:c.1644C>A
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ENSP00000319610.5:p.Ala548=
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|
ENST00000356141.8:c.1740C>A
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ENSP00000348460.4:p.Ala580=
|
|
ENST00000357798.9:c.1701C>A
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ENSP00000350446.5:p.Ala567=
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ENST00000548645.5:c.1650C>A
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ENSP00000448916.1:p.Ala550=
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|
ENST00000551492.5:c.1755C>A
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ENSP00000450392.1:p.Ala585=
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ENST00000551634.5:c.1662C>A
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ENSP00000448373.1:p.Ala554=
|
|
NM_001164749.1:c.1740C>A
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NP_001158221.1:p.Ala580=
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|
NM_001165893.1:c.1650C>A
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NP_001159365.1:p.Ala550=
|
|
NM_022123.2:c.1644C>A
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NP_071406.1:p.Ala548=
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|
NM_173159.2:c.1701C>A
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NP_775182.1:p.Ala567=
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|
XM_005267991.2:c.1761C>A
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XP_005268048.1:p.Ala587=
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XM_005267992.2:c.1755C>A
|
XP_005268049.1:p.Ala585=
|
|
XM_005267993.2:c.1701C>A
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XP_005268050.1:p.Ala567=
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|
XM_011537067.1:c.1791C>A
|
XP_011535369.1:p.Ala597=
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XM_011537068.1:c.1782C>A
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XP_011535370.1:p.Ala594=
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|
XM_011537069.1:c.1752C>A
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XP_011535371.1:p.Ala584=
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|
XM_011537070.1:c.1695C>A
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XP_011535372.1:p.Ala565=
|
|
XM_011537071.1:c.1662C>A
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XP_011535373.1:p.Ala554=
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|
XM_011537072.1:c.1641C>A
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XP_011535374.1:p.Ala547=
|
|
XM_011537073.1:c.1434C>A
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XP_011535375.1:p.Ala478=
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|
XM_011537074.1:c.1434C>A
|
XP_011535376.1:p.Ala478=
|
|
XM_005267991.3:c.1848C>A
|
XP_005268048.2:p.Ala616=
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XM_005267992.3:c.1842C>A
|
XP_005268049.2:p.Ala614=
|
|
XM_011537067.2:c.1791C>A
|
XP_011535369.1:p.Ala597=
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|
XM_011537069.2:c.1839C>A
|
XP_011535371.2:p.Ala613=
|
|
XM_011537070.2:c.1695C>A
|
XP_011535372.1:p.Ala565=
|
|
XM_011537071.2:c.1749C>A
|
XP_011535373.2:p.Ala583=
|
|
XM_011537072.2:c.1641C>A
|
XP_011535374.1:p.Ala547=
|
|
XM_017021582.1:c.1899C>A
|
XP_016877071.1:p.Ala633=
|
|
XM_017021583.1:c.1890C>A
|
XP_016877072.1:p.Ala630=
|
|
XM_017021584.1:c.1809C>A
|
XP_016877073.1:p.Ala603=
|
|
XM_017021585.1:c.1758C>A
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XP_016877074.1:p.Ala586=
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|
XM_017021586.1:c.1434C>A
|
XP_016877075.1:p.Ala478=
|
|
XM_017021587.1:c.1434C>A
|
XP_016877076.1:p.Ala478=
|
|
XM_017021588.1:c.1434C>A
|
XP_016877077.1:p.Ala478=
|
|
NM_001164749.2:c.1740C>A
MANE Select
|
NP_001158221.1:p.Ala580=
|
|
NM_001165893.2:c.1650C>A
|
NP_001159365.1:p.Ala550=
|
|
NM_022123.3:c.1644C>A
|
NP_071406.1:p.Ala548=
|
|
NM_173159.3:c.1701C>A
|
NP_775182.1:p.Ala567=
|
|
NM_001394988.1:c.1695C>A
|
NP_001381917.1:p.Ala565=
|
|
NM_001394989.1:c.1641C>A
|
NP_001381918.1:p.Ala547=
|
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