|
ENST00000689298.1:c.*1698C>T
|
ENSP00000508434.1:n.*1698C>T
|
|
|
ENST00000440875.6:c.1072C>T
|
ENSP00000475553.3:p.His358Tyr
|
|
|
ENST00000627532.3:c.1849C>T
MANE Select
|
ENSP00000487174.1:p.His617Tyr
|
|
|
ENST00000636026.2:c.1849C>T
|
ENSP00000490776.1:p.His617Tyr
|
|
|
ENST00000636179.1:n.1818C>T
|
|
|
|
ENST00000636413.1:c.1513C>T
|
ENSP00000490508.1:p.His505Tyr
|
|
|
ENST00000636471.1:c.1924C>T
|
ENSP00000490317.1:p.His642Tyr
|
|
|
ENST00000636732.2:c.*1566C>T
|
ENSP00000490175.1:n.*1566C>T
|
|
|
ENST00000636820.1:n.1949C>T
|
|
|
|
ENST00000637045.1:c.1513C>T
|
ENSP00000490141.1:p.His505Tyr
|
|
|
ENST00000637304.1:c.1513C>T
|
ENSP00000490872.1:p.His505Tyr
|
|
|
ENST00000638007.1:c.1513C>T
|
ENSP00000490723.1:p.His505Tyr
|
|
|
ENST00000638087.1:c.1513C>T
|
ENSP00000490673.1:p.His505Tyr
|
|
|
ENST00000638128.1:c.1072C>T
|
ENSP00000490934.1:p.His358Tyr
|
|
|
ENST00000675069.1:c.-133-488C>T
|
ENSP00000502467.1:n.-133-488C>T
|
|
|
ENST00000675145.1:n.2397C>T
|
|
|
|
ENST00000303660.8:c.1846C>T
|
ENSP00000302501.4:p.His616Tyr
|
|
|
ENST00000409487.7:c.1849C>T
|
ENSP00000386854.2:p.His617Tyr
|
|
|
ENST00000419938.5:c.655+1861C>T
|
ENSP00000394777.2:n.655+1861C>T
|
|
|
ENST00000427902.5:c.1936C>T
|
ENSP00000395496.2:p.His646Tyr
|
|
|
ENST00000440875.5:c.1167+199C>T
|
ENSP00000475553.2:n.1167+199C>T
|
|
|
ENST00000539609.7:c.1777C>T
|
ENSP00000443792.2:p.His593Tyr
|
|
|
ENST00000558170.6:c.1849C>T
|
ENSP00000454157.1:p.His617Tyr
|
|
|
ENST00000627532.2:c.1849C>T
|
ENSP00000487174.1:p.His617Tyr
|
|
|
NM_001171653.1:c.1777C>T
|
NP_001165124.1:p.His593Tyr
|
|
|
NM_014795.3:c.1849C>T
|
NP_055610.1:p.His617Tyr
|
|
|
XM_006712881.2:c.1849C>T
|
XP_006712944.1:p.His617Tyr
|
|
|
XM_006712882.2:c.1849C>T
|
XP_006712945.1:p.His617Tyr
|
|
|
XM_011512231.1:c.1840C>T
|
XP_011510533.1:p.His614Tyr
|
|
|
XM_011512232.1:c.1828C>T
|
XP_011510534.1:p.His610Tyr
|
|
|
NM_014795.4:c.1849C>T
MANE Select
|
NP_055610.1:p.His617Tyr
|
|
|
NM_001171653.2:c.1777C>T
|
NP_001165124.1:p.His593Tyr
|
|
