|
ENST00000348911.11:c.5429C>G
|
ENSP00000252027.8:p.Ala1810Gly
|
|
|
ENST00000418590.4:c.1103C>G
|
ENSP00000401538.2:p.Ala368Gly
|
|
|
ENST00000470434.2:n.1910C>G
|
|
|
|
ENST00000473724.2:n.646C>G
|
|
|
|
ENST00000684986.1:c.5510C>G
|
ENSP00000509117.1:p.Ala1837Gly
|
|
|
ENST00000685180.1:n.3118C>G
|
|
|
|
ENST00000685390.1:n.3458C>G
|
|
|
|
ENST00000685411.1:n.1880C>G
|
|
|
|
ENST00000685459.1:c.659C>G
|
ENSP00000509511.1:p.Ala220Gly
|
|
|
ENST00000685592.1:c.1757C>G
|
|
|
|
ENST00000685809.1:c.5420C>G
|
ENSP00000508863.1:p.Ala1807Gly
|
|
|
ENST00000686191.1:n.4707C>G
|
|
|
|
ENST00000686222.1:c.*4929C>G
|
ENSP00000508737.1:n.*4929C>G
|
|
|
ENST00000686321.1:c.1820C>G
|
|
|
|
ENST00000686427.1:c.*2439C>G
|
ENSP00000510379.1:n.*2439C>G
|
|
|
ENST00000686758.1:n.3321C>G
|
|
|
|
ENST00000686801.1:c.*345C>G
|
ENSP00000509915.1:n.*345C>G
|
|
|
ENST00000686826.1:n.1826C>G
|
|
|
|
ENST00000687016.1:c.5405C>G
|
ENSP00000509074.1:p.Ala1802Gly
|
|
|
ENST00000687704.1:c.*3303C>G
|
ENSP00000510454.1:n.*3303C>G
|
|
|
ENST00000688066.1:c.5507C>G
|
ENSP00000510782.1:p.Ala1836Gly
|
|
|
ENST00000688124.1:c.*4408C>G
|
ENSP00000510645.1:n.*4408C>G
|
|
|
ENST00000688381.1:c.628C>G
|
ENSP00000508847.1:p.Arg210Gly
|
|
|
ENST00000688848.1:c.*4851C>G
|
ENSP00000509419.1:n.*4851C>G
|
|
|
ENST00000688985.1:c.2508C>G
|
ENSP00000510477.1:n.2508C>G
|
|
|
ENST00000689129.1:c.5432C>G
|
ENSP00000510414.1:p.Ala1811Gly
|
|
|
ENST00000689177.1:n.6844C>G
|
|
|
|
ENST00000689849.1:c.1592C>G
|
|
|
|
ENST00000689981.1:c.5507C>G
|
ENSP00000509035.1:p.Ala1836Gly
|
|
|
ENST00000690197.1:c.25C>G
|
|
|
|
ENST00000690369.1:n.5525C>G
|
|
|
|
ENST00000690590.1:n.2554C>G
|
|
|
|
ENST00000690990.1:c.5501C>G
|
ENSP00000510461.1:p.Ala1834Gly
|
|
|
ENST00000691233.1:c.5426C>G
|
ENSP00000509215.1:p.Ala1809Gly
|
|
|
ENST00000691345.1:n.2834C>G
|
|
|
|
ENST00000691792.1:c.5492C>G
|
ENSP00000509911.1:p.Ala1831Gly
|
|
|
ENST00000691959.1:n.6849C>G
|
|
|
|
ENST00000692844.1:n.2591C>G
|
|
|
|
ENST00000692946.1:c.1603C>G
|
|
|
|
ENST00000693052.1:c.5525C>G
|
ENSP00000509558.1:p.Ala1842Gly
|
|
|
ENST00000693068.1:c.590C>G
|
ENSP00000509997.1:p.Ala197Gly
|
|
|
ENST00000693440.1:c.5504C>G
|
ENSP00000509462.1:p.Ala1835Gly
|
|
|
ENST00000693591.1:n.4315C>G
|
|
|
|
ENST00000380817.8:c.5507C>G
MANE Select
|
ENSP00000370196.2:p.Ala1836Gly
|
|
|
ENST00000348911.10:c.5432C>G
|
ENSP00000252027.7:p.Ala1811Gly
|
|
|
ENST00000380817.7:c.5507C>G
|
ENSP00000370196.2:p.Ala1836Gly
|
|
|
ENST00000418590.3:c.1071C>G
|
|
|
|
ENST00000470434.1:n.1648C>G
|
|
|
|
ENST00000473724.1:n.212C>G
|
|
|
|
NM_002972.3:c.5507C>G
|
NP_002963.2:p.Ala1836Gly
|
|
|
XM_005261931.1:c.5510C>G
|
XP_005261988.1:p.Ala1837Gly
|
|
|
XM_005261935.1:c.5429C>G
|
XP_005261992.1:p.Ala1810Gly
|
|
|
XM_011530707.1:c.5609C>G
|
XP_011529009.1:p.Ala1870Gly
|
|
|
XM_011530708.1:c.5561C>G
|
XP_011529010.1:p.Ala1854Gly
|
|
|
XM_011530709.1:c.5537C>G
|
XP_011529011.1:p.Ala1846Gly
|
|
|
XM_011530710.1:c.5534C>G
|
XP_011529012.1:p.Ala1845Gly
|
|
|
XM_011530711.1:c.5534C>G
|
XP_011529013.1:p.Ala1845Gly
|
|
|
XR_938344.1:n.5627C>G
|
|
|
|
NM_001365819.1:c.5432C>G
|
NP_001352748.1:p.Ala1811Gly
|
|
|
XM_005261935.2:c.5429C>G
|
XP_005261992.1:p.Ala1810Gly
|
|
|
XM_011530709.2:c.5537C>G
|
XP_011529011.1:p.Ala1846Gly
|
|
|
XM_011530710.2:c.5534C>G
|
XP_011529012.1:p.Ala1845Gly
|
|
|
XM_017028905.2:c.5459C>G
|
XP_016884394.1:p.Ala1820Gly
|
|
|
NM_002972.4:c.5507C>G
MANE Select
|
NP_002963.2:p.Ala1836Gly
|
|
