ENST00000685097.1:c.4220A>T
|
ENSP00000510510.1:p.Asp1407Val
|
|
ENST00000686383.1:n.4402A>T
|
|
|
ENST00000686906.1:c.*405A>T
|
ENSP00000508907.1:n.*405A>T
|
|
ENST00000687894.1:c.*1889A>T
|
ENSP00000509577.1:n.*1889A>T
|
|
ENST00000687912.1:c.4022A>T
|
ENSP00000508455.1:p.Asp1341Val
|
|
ENST00000689369.1:c.3882+1925A>T
|
ENSP00000509856.1:n.3882+1925A>T
|
|
ENST00000689852.1:c.3915+1925A>T
|
ENSP00000510537.1:n.3915+1925A>T
|
|
ENST00000691030.1:c.4496A>T
|
ENSP00000510148.1:p.Asp1499Val
|
|
ENST00000693394.1:c.3882+1925A>T
|
ENSP00000509014.1:n.3882+1925A>T
|
|
ENST00000693432.1:c.4053+1925A>T
|
ENSP00000510486.1:n.4053+1925A>T
|
|
ENST00000693597.1:n.861+1925A>T
|
|
|
ENST00000256707.8:c.4517A>T
MANE Select
|
ENSP00000256707.4:p.Asp1506Val
|
|
ENST00000569008.2:c.3882+1925A>T
|
ENSP00000491461.1:n.3882+1925A>T
|
|
ENST00000256707.7:c.4517A>T
|
ENSP00000256707.3:p.Asp1506Val
|
|
ENST00000473731.5:c.4460A>T
|
ENSP00000418974.1:p.Asp1487Val
|
|
ENST00000488729.5:c.*4406A>T
|
ENSP00000417390.1:n.*4406A>T
|
|
ENST00000496383.5:c.3123+1925A>T
|
ENSP00000420364.1:n.3123+1925A>T
|
|
NM_020738.2:c.4517A>T
|
NP_065789.1:p.Asp1506Val
|
|
NM_001348729.1:c.4520A>T
|
NP_001335658.1:p.Asp1507Val
|
|
NM_001348731.1:c.4463A>T
|
NP_001335660.1:p.Asp1488Val
|
|
NM_001348732.1:c.4460A>T
|
NP_001335661.1:p.Asp1487Val
|
|
NM_001348734.1:c.4349A>T
|
NP_001335663.1:p.Asp1450Val
|
|
NM_001348735.1:c.4346A>T
|
NP_001335664.1:p.Asp1449Val
|
|
NM_001348736.1:c.4220A>T
|
NP_001335665.1:p.Asp1407Val
|
|
NM_001348738.1:c.3996+1925A>T
|
NP_001335667.1:n.3996+1925A>T
|
|
NM_001348739.1:c.3885+1925A>T
|
NP_001335668.1:n.3885+1925A>T
|
|
NM_001348740.1:c.3885+1925A>T
|
NP_001335669.1:n.3885+1925A>T
|
|
NM_001348741.1:c.3882+1925A>T
|
NP_001335670.1:n.3882+1925A>T
|
|
NM_001348742.1:c.3882+1925A>T
|
NP_001335671.1:n.3882+1925A>T
|
|
NM_001348743.1:c.3882+1925A>T
|
NP_001335672.1:n.3882+1925A>T
|
|
NM_020738.3:c.4517A>T
|
NP_065789.1:p.Asp1506Val
|
|
NR_145964.1:n.4252+1925A>T
|
|
|
NR_145965.1:n.4078+1925A>T
|
|
|
NM_001348729.2:c.4520A>T
|
NP_001335658.1:p.Asp1507Val
|
|
NM_001348731.2:c.4463A>T
|
NP_001335660.1:p.Asp1488Val
|
|
NM_001348732.2:c.4460A>T
|
NP_001335661.1:p.Asp1487Val
|
|
NM_001348734.2:c.4349A>T
|
NP_001335663.1:p.Asp1450Val
|
|
NM_001348735.2:c.4346A>T
|
NP_001335664.1:p.Asp1449Val
|
|
NM_001348736.2:c.4220A>T
|
NP_001335665.1:p.Asp1407Val
|
|
NM_001348738.2:c.3996+1925A>T
|
NP_001335667.1:n.3996+1925A>T
|
|
NM_001348739.2:c.3885+1925A>T
|
NP_001335668.1:n.3885+1925A>T
|
|
NM_001348740.2:c.3885+1925A>T
|
NP_001335669.1:n.3885+1925A>T
|
|
NM_001348741.2:c.3882+1925A>T
|
NP_001335670.1:n.3882+1925A>T
|
|
NM_001348742.2:c.3882+1925A>T
|
NP_001335671.1:n.3882+1925A>T
|
|
NM_001348743.2:c.3882+1925A>T
|
NP_001335672.1:n.3882+1925A>T
|
|
NM_020738.4:c.4517A>T
MANE Select
|
NP_065789.1:p.Asp1506Val
|
|
NR_145964.2:n.4226+1925A>T
|
|
|
NR_145965.2:n.4052+1925A>T
|
|
|