|
ENST00000348127.11:c.788A>T
|
ENSP00000265385.8:p.Asp263Val
|
|
|
ENST00000484496.6:n.771A>T
|
|
|
|
ENST00000338791.11:c.896A>T
MANE Select
|
ENSP00000345096.6:p.Asp299Val
|
|
|
ENST00000648462.1:c.528A>T
|
|
|
|
ENST00000338791.10:c.896A>T
|
ENSP00000345096.6:p.Asp299Val
|
|
|
ENST00000348127.10:c.788A>T
|
ENSP00000265385.8:p.Asp263Val
|
|
|
ENST00000354269.9:c.866A>T
|
ENSP00000346219.5:p.Asp289Val
|
|
|
ENST00000419067.6:c.797A>T
|
ENSP00000399400.2:p.Asp266Val
|
|
|
ENST00000468842.1:n.485A>T
|
|
|
|
ENST00000469328.5:c.661A>T
|
|
|
|
ENST00000470772.5:c.638A>T
|
ENSP00000417296.1:p.Asp213Val
|
|
|
ENST00000480861.5:c.626A>T
|
ENSP00000420185.1:p.Asp209Val
|
|
|
ENST00000484496.5:c.771A>T
|
ENSP00000418742.1:n.771A>T
|
|
|
ENST00000496200.5:c.566A>T
|
ENSP00000420803.1:p.Asp189Val
|
|
|
ENST00000497868.5:c.689A>T
|
ENSP00000419609.1:p.Asp230Val
|
|
|
ENST00000626419.2:c.638A>T
|
ENSP00000486056.1:p.Asp213Val
|
|
|
NM_000883.3:c.896A>T
|
NP_000874.2:p.Asp299Val
|
|
|
NM_001102605.1:c.866A>T
|
NP_001096075.1:p.Asp289Val
|
|
|
NM_001142573.1:c.641A>T
|
NP_001136045.1:p.Asp214Val
|
|
|
NM_001142574.1:c.626A>T
|
NP_001136046.1:p.Asp209Val
|
|
|
NM_001142575.1:c.566A>T
|
NP_001136047.1:p.Asp189Val
|
|
|
NM_001142576.1:c.797A>T
|
NP_001136048.1:p.Asp266Val
|
|
|
NM_001304521.1:c.689A>T
|
NP_001291450.1:p.Asp230Val
|
|
|
NM_183243.2:c.788A>T
|
NP_899066.1:p.Asp263Val
|
|
|
XM_005250314.1:c.665A>T
|
XP_005250371.1:p.Asp222Val
|
|
|
XM_006715967.1:c.896A>T
|
XP_006716030.1:p.Asp299Val
|
|
|
XM_006715968.1:c.866A>T
|
XP_006716031.1:p.Asp289Val
|
|
|
XM_006715969.1:c.788A>T
|
XP_006716032.1:p.Asp263Val
|
|
|
XM_006715970.2:c.689A>T
|
XP_006716033.1:p.Asp230Val
|
|
|
XM_006715971.1:c.665A>T
|
XP_006716034.1:p.Asp222Val
|
|
|
XM_011516156.1:c.278A>T
|
XP_011514458.1:p.Asp93Val
|
|
|
XM_011516157.1:c.278A>T
|
XP_011514459.1:p.Asp93Val
|
|
|
XM_017012172.1:c.665A>T
|
XP_016867661.1:p.Asp222Val
|
|
|
XM_017012173.1:c.866A>T
|
XP_016867662.1:p.Asp289Val
|
|
|
XM_024446755.1:c.866A>T
|
XP_024302523.1:p.Asp289Val
|
|
|
XM_024446756.1:c.788A>T
|
XP_024302524.1:p.Asp263Val
|
|
|
XM_024446757.1:c.689A>T
|
XP_024302525.1:p.Asp230Val
|
|
|
XM_024446758.1:c.665A>T
|
XP_024302526.1:p.Asp222Val
|
|
|
NM_000883.4:c.896A>T
MANE Select
|
NP_000874.2:p.Asp299Val
|
|
|
NM_001102605.2:c.866A>T
|
NP_001096075.1:p.Asp289Val
|
|
|
NM_001142573.2:c.641A>T
|
NP_001136045.1:p.Asp214Val
|
|
|
NM_001142574.2:c.626A>T
|
NP_001136046.1:p.Asp209Val
|
|
|
NM_001142575.2:c.566A>T
|
NP_001136047.1:p.Asp189Val
|
|
|
NM_001142576.2:c.797A>T
|
NP_001136048.1:p.Asp266Val
|
|
|
NM_001304521.2:c.689A>T
|
NP_001291450.1:p.Asp230Val
|
|
|
NM_183243.3:c.788A>T
|
NP_899066.1:p.Asp263Val
|
|
