ENST00000356141.9:c.2213C>T
MANE Select
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ENSP00000348460.4:p.Ala738Val
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ENST00000551634.6:c.2222C>T
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ENSP00000448373.2:p.Ala741Val
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ENST00000680362.1:c.2113C>T
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ENST00000681323.1:c.793+2939C>T
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ENST00000346562.6:c.2117C>T
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ENSP00000319610.5:p.Ala706Val
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ENST00000356141.8:c.2213C>T
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ENSP00000348460.4:p.Ala738Val
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ENST00000357798.9:c.2174C>T
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ENSP00000350446.5:p.Ala725Val
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ENST00000548645.5:c.2123C>T
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ENSP00000448916.1:p.Ala708Val
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ENST00000551492.5:c.2228C>T
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ENSP00000450392.1:p.Ala743Val
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ENST00000551634.5:c.2135C>T
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ENSP00000448373.1:p.Ala712Val
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NM_001164749.1:c.2213C>T
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NP_001158221.1:p.Ala738Val
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NM_001165893.1:c.2123C>T
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NP_001159365.1:p.Ala708Val
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NM_022123.2:c.2117C>T
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NP_071406.1:p.Ala706Val
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NM_173159.2:c.2174C>T
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NP_775182.1:p.Ala725Val
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XM_005267991.2:c.2234C>T
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XP_005268048.1:p.Ala745Val
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XM_005267992.2:c.2228C>T
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XP_005268049.1:p.Ala743Val
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XM_005267993.2:c.2174C>T
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XP_005268050.1:p.Ala725Val
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XM_011537067.1:c.2264C>T
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XP_011535369.1:p.Ala755Val
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XM_011537068.1:c.2255C>T
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XP_011535370.1:p.Ala752Val
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XM_011537069.1:c.2225C>T
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XP_011535371.1:p.Ala742Val
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XM_011537070.1:c.2168C>T
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XP_011535372.1:p.Ala723Val
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XM_011537071.1:c.2135C>T
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XP_011535373.1:p.Ala712Val
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XM_011537072.1:c.2114C>T
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XP_011535374.1:p.Ala705Val
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XM_011537073.1:c.1907C>T
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XP_011535375.1:p.Ala636Val
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XM_011537074.1:c.1907C>T
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XP_011535376.1:p.Ala636Val
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XM_005267991.3:c.2321C>T
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XP_005268048.2:p.Ala774Val
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XM_005267992.3:c.2315C>T
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XP_005268049.2:p.Ala772Val
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XM_011537067.2:c.2264C>T
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XP_011535369.1:p.Ala755Val
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XM_011537069.2:c.2312C>T
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XP_011535371.2:p.Ala771Val
|
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XM_011537070.2:c.2168C>T
|
XP_011535372.1:p.Ala723Val
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XM_011537071.2:c.2222C>T
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XP_011535373.2:p.Ala741Val
|
|
XM_011537072.2:c.2114C>T
|
XP_011535374.1:p.Ala705Val
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XM_017021582.1:c.2372C>T
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XP_016877071.1:p.Ala791Val
|
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XM_017021583.1:c.2363C>T
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XP_016877072.1:p.Ala788Val
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XM_017021584.1:c.2282C>T
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XP_016877073.1:p.Ala761Val
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XM_017021585.1:c.2231C>T
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XP_016877074.1:p.Ala744Val
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XM_017021586.1:c.1907C>T
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XP_016877075.1:p.Ala636Val
|
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XM_017021587.1:c.1907C>T
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XP_016877076.1:p.Ala636Val
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XM_017021588.1:c.1907C>T
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XP_016877077.1:p.Ala636Val
|
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NM_001164749.2:c.2213C>T
MANE Select
|
NP_001158221.1:p.Ala738Val
|
|
NM_001165893.2:c.2123C>T
|
NP_001159365.1:p.Ala708Val
|
|
NM_022123.3:c.2117C>T
|
NP_071406.1:p.Ala706Val
|
|
NM_173159.3:c.2174C>T
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NP_775182.1:p.Ala725Val
|
|
NM_001394988.1:c.2168C>T
|
NP_001381917.1:p.Ala723Val
|
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NM_001394989.1:c.2114C>T
|
NP_001381918.1:p.Ala705Val
|
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