|
ENST00000478464.6:c.568G>T
|
ENSP00000419303.2:p.Asp190Tyr
|
|
|
ENST00000480644.2:c.694G>T
|
ENSP00000420229.2:p.Asp232Tyr
|
|
|
ENST00000492644.2:n.3032G>T
|
|
|
|
ENST00000684961.1:c.397G>T
|
ENSP00000508439.1:p.Asp133Tyr
|
|
|
ENST00000686433.1:c.724G>T
|
ENSP00000509173.1:p.Asp242Tyr
|
|
|
ENST00000687538.1:c.568G>T
|
ENSP00000508887.1:p.Asp190Tyr
|
|
|
ENST00000688697.1:c.778G>T
|
ENSP00000510396.1:p.Asp260Tyr
|
|
|
ENST00000689286.1:c.568G>T
|
ENSP00000509897.1:p.Asp190Tyr
|
|
|
ENST00000689925.1:c.*119G>T
|
ENSP00000510082.1:n.*119G>T
|
|
|
ENST00000690298.1:c.*419G>T
|
ENSP00000509376.1:n.*419G>T
|
|
|
ENST00000691070.1:c.694G>T
|
ENSP00000509723.1:p.Asp232Tyr
|
|
|
ENST00000692727.1:n.3300G>T
|
|
|
|
ENST00000693155.1:n.1455G>T
|
|
|
|
ENST00000310776.9:c.775G>T
|
ENSP00000310785.5:p.Asp259Tyr
|
|
|
ENST00000680020.1:c.778G>T
MANE Select
|
ENSP00000505414.1:p.Asp260Tyr
|
|
|
ENST00000310776.8:c.778G>T
|
ENSP00000310785.4:p.Asp260Tyr
|
|
|
ENST00000465056.5:c.775G>T
|
ENSP00000418233.1:p.Asp259Tyr
|
|
|
ENST00000478464.5:c.655G>T
|
ENSP00000419303.1:p.Asp219Tyr
|
|
|
ENST00000480644.1:c.263G>T
|
|
|
|
ENST00000480938.5:n.1432G>T
|
|
|
|
ENST00000492644.1:n.1823G>T
|
|
|
|
ENST00000495075.5:c.778G>T
|
ENSP00000418008.1:p.Asp260Tyr
|
|
|
ENST00000498505.5:c.*375G>T
|
ENSP00000420482.1:n.*375G>T
|
|
|
NM_020191.2:c.778G>T
|
NP_064576.1:p.Asp260Tyr
|
|
|
XM_005247640.2:c.775G>T
|
XP_005247697.1:p.Asp259Tyr
|
|
|
XM_006713703.2:c.724G>T
|
XP_006713766.1:p.Asp242Tyr
|
|
|
XM_011512995.1:c.655G>T
|
XP_011511297.1:p.Asp219Tyr
|
|
|
XM_011512996.1:c.652G>T
|
XP_011511298.1:p.Asp218Tyr
|
|
|
NM_001363857.1:c.655G>T
|
NP_001350786.1:p.Asp219Tyr
|
|
|
NM_001363893.1:c.775G>T
|
NP_001350822.1:p.Asp259Tyr
|
|
|
NM_020191.3:c.778G>T
|
NP_064576.1:p.Asp260Tyr
|
|
|
XM_006713703.4:c.724G>T
|
XP_006713766.1:p.Asp242Tyr
|
|
|
XM_011512996.2:c.652G>T
|
XP_011511298.1:p.Asp218Tyr
|
|
|
NM_020191.4:c.778G>T
MANE Select
|
NP_064576.1:p.Asp260Tyr
|
|
