|
ENST00000348911.11:c.4478T>G
|
ENSP00000252027.8:p.Val1493Gly
|
|
|
ENST00000418590.4:c.188T>G
|
ENSP00000401538.2:p.Val63Gly
|
|
|
ENST00000470434.2:n.959T>G
|
|
|
|
ENST00000684986.1:c.4559T>G
|
ENSP00000509117.1:p.Val1520Gly
|
|
|
ENST00000685180.1:n.2488+5393T>G
|
|
|
|
ENST00000685390.1:n.2524T>G
|
|
|
|
ENST00000685411.1:n.306T>G
|
|
|
|
ENST00000685592.1:c.790T>G
|
|
|
|
ENST00000685809.1:c.4469T>G
|
ENSP00000508863.1:p.Val1490Gly
|
|
|
ENST00000686029.1:c.634T>G
|
|
|
|
ENST00000686191.1:n.3756T>G
|
|
|
|
ENST00000686222.1:c.*3978T>G
|
ENSP00000508737.1:n.*3978T>G
|
|
|
ENST00000686321.1:c.652T>G
|
|
|
|
ENST00000686427.1:c.*1491T>G
|
ENSP00000510379.1:n.*1491T>G
|
|
|
ENST00000686758.1:n.2299T>G
|
|
|
|
ENST00000686801.1:c.4544T>G
|
ENSP00000509915.1:p.Val1515Gly
|
|
|
ENST00000686826.1:n.875T>G
|
|
|
|
ENST00000687016.1:c.4457T>G
|
ENSP00000509074.1:p.Val1486Gly
|
|
|
ENST00000687704.1:c.*2281T>G
|
ENSP00000510454.1:n.*2281T>G
|
|
|
ENST00000688066.1:c.4556T>G
|
ENSP00000510782.1:p.Val1519Gly
|
|
|
ENST00000688124.1:c.*3474T>G
|
ENSP00000510645.1:n.*3474T>G
|
|
|
ENST00000688848.1:c.*3900T>G
|
ENSP00000509419.1:n.*3900T>G
|
|
|
ENST00000688985.1:c.1557T>G
|
ENSP00000510477.1:n.1557T>G
|
|
|
ENST00000689129.1:c.4481T>G
|
ENSP00000510414.1:p.Val1494Gly
|
|
|
ENST00000689177.1:n.5828T>G
|
|
|
|
ENST00000689849.1:c.652T>G
|
|
|
|
ENST00000689981.1:c.4556T>G
|
ENSP00000509035.1:p.Val1519Gly
|
|
|
ENST00000690369.1:n.4574T>G
|
|
|
|
ENST00000690590.1:n.1603T>G
|
|
|
|
ENST00000690990.1:c.4550T>G
|
ENSP00000510461.1:p.Val1517Gly
|
|
|
ENST00000691233.1:c.4475T>G
|
ENSP00000509215.1:p.Val1492Gly
|
|
|
ENST00000691306.1:c.654T>G
|
|
|
|
ENST00000691345.1:n.2302+1075T>G
|
|
|
|
ENST00000691792.1:c.4555-11T>G
|
ENSP00000509911.1:n.4555-11T>G
|
|
|
ENST00000691959.1:n.5275T>G
|
|
|
|
ENST00000692844.1:n.1640T>G
|
|
|
|
ENST00000692946.1:c.652T>G
|
|
|
|
ENST00000693052.1:c.4574T>G
|
ENSP00000509558.1:p.Val1525Gly
|
|
|
ENST00000693289.1:n.1715T>G
|
|
|
|
ENST00000693440.1:c.4553T>G
|
ENSP00000509462.1:p.Val1518Gly
|
|
|
ENST00000693499.1:n.5481T>G
|
|
|
|
ENST00000693591.1:n.3293T>G
|
|
|
|
ENST00000380817.8:c.4556T>G
MANE Select
|
ENSP00000370196.2:p.Val1519Gly
|
|
|
ENST00000348911.10:c.4481T>G
|
ENSP00000252027.7:p.Val1494Gly
|
|
|
ENST00000380817.7:c.4556T>G
|
ENSP00000370196.2:p.Val1519Gly
|
|
|
ENST00000418590.3:c.156T>G
|
|
|
|
ENST00000470434.1:n.697T>G
|
|
|
|
NM_002972.3:c.4556T>G
|
NP_002963.2:p.Val1519Gly
|
|
|
XM_005261931.1:c.4559T>G
|
XP_005261988.1:p.Val1520Gly
|
|
|
XM_005261935.1:c.4478T>G
|
XP_005261992.1:p.Val1493Gly
|
|
|
XM_011530707.1:c.4658T>G
|
XP_011529009.1:p.Val1553Gly
|
|
|
XM_011530708.1:c.4610T>G
|
XP_011529010.1:p.Val1537Gly
|
|
|
XM_011530709.1:c.4586T>G
|
XP_011529011.1:p.Val1529Gly
|
|
|
XM_011530710.1:c.4583T>G
|
XP_011529012.1:p.Val1528Gly
|
|
|
XM_011530711.1:c.4583T>G
|
XP_011529013.1:p.Val1528Gly
|
|
|
XR_938344.1:n.4676T>G
|
|
|
|
NM_001365819.1:c.4481T>G
|
NP_001352748.1:p.Val1494Gly
|
|
|
XM_005261935.2:c.4478T>G
|
XP_005261992.1:p.Val1493Gly
|
|
|
XM_011530709.2:c.4586T>G
|
XP_011529011.1:p.Val1529Gly
|
|
|
XM_011530710.2:c.4583T>G
|
XP_011529012.1:p.Val1528Gly
|
|
|
XM_017028905.2:c.4508T>G
|
XP_016884394.1:p.Val1503Gly
|
|
|
NM_002972.4:c.4556T>G
MANE Select
|
NP_002963.2:p.Val1519Gly
|
|
