ENST00000268704.7:c.1944C>G
|
ENSP00000268704.3:p.Thr648=
|
|
ENST00000561702.6:n.2637C>G
|
|
|
ENST00000566682.2:c.1006C>G
|
ENSP00000461979.2:p.Pro336Ala
|
|
ENST00000569720.2:n.648C>G
|
|
|
ENST00000569820.6:c.2238C>G
|
|
|
ENST00000642226.1:n.2028C>G
|
|
|
ENST00000642334.1:c.3383C>G
|
|
|
ENST00000642814.1:n.1380C>G
|
|
|
ENST00000642984.1:n.1688C>G
|
|
|
ENST00000643105.1:c.2671C>G
|
|
|
ENST00000643350.1:n.1379C>G
|
|
|
ENST00000643409.1:n.2390C>G
|
|
|
ENST00000643496.1:n.1782C>G
|
|
|
ENST00000643649.1:c.1854C>G
|
ENSP00000494806.1:p.Thr618=
|
|
ENST00000643668.1:c.*2259C>G
|
ENSP00000494903.1:n.*2259C>G
|
|
ENST00000643724.1:c.*1013C>G
|
ENSP00000496335.1:n.*1013C>G
|
|
ENST00000643954.1:c.2864C>G
|
|
|
ENST00000644171.1:n.2725C>G
|
|
|
ENST00000644210.1:c.*537C>G
|
ENSP00000495675.1:n.*537C>G
|
|
ENST00000644225.1:n.1982C>G
|
|
|
ENST00000644281.1:n.2649C>G
|
|
|
ENST00000644464.1:n.618C>G
|
|
|
ENST00000644498.1:c.*1784C>G
|
ENSP00000496244.1:n.*1784C>G
|
|
ENST00000644671.1:c.1622C>G
|
|
|
ENST00000644751.1:c.1153C>G
|
|
|
ENST00000644781.1:c.1920C>G
|
ENSP00000495473.1:p.Thr640=
|
|
ENST00000644901.1:c.*2359C>G
|
ENSP00000493797.1:n.*2359C>G
|
|
ENST00000645042.1:c.*739C>G
|
ENSP00000493908.1:n.*739C>G
|
|
ENST00000645063.1:c.1965C>G
|
ENSP00000493590.1:p.Thr655=
|
|
ENST00000645354.1:c.2725C>G
|
|
|
ENST00000645392.1:n.2306C>G
|
|
|
ENST00000645742.1:n.599C>G
|
|
|
ENST00000645818.2:c.1965C>G
MANE Select
|
ENSP00000495795.2:p.Thr655=
|
|
ENST00000645842.1:n.1810C>G
|
|
|
ENST00000645886.1:c.1470C>G
|
|
|
ENST00000645897.1:c.1503C>G
|
ENSP00000495293.1:p.Thr501=
|
|
ENST00000645952.1:n.1830C>G
|
|
|
ENST00000645977.1:n.3083C>G
|
|
|
ENST00000646005.1:n.1723C>G
|
|
|
ENST00000646263.1:c.*838C>G
|
ENSP00000494119.1:n.*838C>G
|
|
ENST00000646303.1:c.1833C>G
|
ENSP00000494160.1:p.Thr611=
|
|
ENST00000646399.1:c.2859C>G
|
|
|
ENST00000646445.1:c.823C>G
|
|
|
ENST00000646531.1:c.*588C>G
|
ENSP00000495185.1:n.*588C>G
|
|
ENST00000646589.1:c.*1093C>G
|
ENSP00000494739.1:n.*1093C>G
|
|
ENST00000646716.1:c.1017C>G
|
ENSP00000495593.1:p.Thr339=
|
|
ENST00000646826.1:c.*638C>G
|
ENSP00000495123.1:n.*638C>G
|
|
ENST00000646930.1:c.*1894C>G
|
ENSP00000495219.1:n.*1894C>G
|
|
ENST00000647032.1:c.1580C>G
|
|
|
ENST00000647079.1:c.1557C>G
|
ENSP00000495967.1:p.Thr519=
|
|
ENST00000647123.1:n.1922C>G
|
|
|
ENST00000647227.1:c.1603C>G
|
|
|
ENST00000647302.1:n.2615C>G
|
|
|
ENST00000647476.1:n.852C>G
|
|
|
ENST00000647491.1:n.1709C>G
|
|
|
ENST00000268704.6:c.1965C>G
|
ENSP00000268704.2:p.Thr655=
|
|
ENST00000561702.5:n.950C>G
|
|
|
ENST00000561911.5:c.565C>G
|
ENSP00000457387.1:p.Pro189Ala
|
|
ENST00000566682.1:c.101C>G
|
|
|
ENST00000569720.1:n.156C>G
|
|
|
ENST00000569820.5:c.1207C>G
|
|
|
ENST00000620811.4:c.*11C>G
|
ENSP00000478030.1:n.*11C>G
|
|
NM_003119.3:c.1965C>G
|
NP_003110.1:p.Thr655=
|
|
XM_006721264.2:c.1965C>G
|
XP_006721327.1:p.Thr655=
|
|
NM_001363850.1:c.1965C>G
|
NP_001350779.1:p.Thr655=
|
|
XM_006721264.4:c.1965C>G
|
XP_006721327.1:p.Thr655=
|
|
XR_001751971.2:n.2314C>G
|
|
|
XR_001751972.2:n.3601C>G
|
|
|
NM_003119.4:c.1965C>G
MANE Select
|
NP_003110.1:p.Thr655=
|
|