ENST00000376091.8:c.1016T>A
MANE Select
|
ENSP00000365259.3:p.Val339Asp
|
|
ENST00000642383.1:c.266T>A
|
ENSP00000496353.1:p.Val89Asp
|
|
ENST00000642885.1:c.806T>A
|
ENSP00000496632.1:p.Val269Asp
|
|
ENST00000643129.1:c.1303T>A
|
|
|
ENST00000646398.1:c.*191T>A
|
ENSP00000495122.1:n.*191T>A
|
|
ENST00000307367.2:c.806T>A
|
ENSP00000304257.2:p.Val269Asp
|
|
ENST00000376088.7:c.1016T>A
|
ENSP00000365256.3:p.Val339Asp
|
|
ENST00000376091.7:c.1016T>A
|
ENSP00000365259.3:p.Val339Asp
|
|
ENST00000376108.7:c.806T>A
|
ENSP00000365276.3:p.Val269Asp
|
|
NM_000084.4:c.806T>A
|
NP_000075.1:p.Val269Asp
|
|
NM_001127898.3:c.1016T>A
|
NP_001121370.1:p.Val339Asp
|
|
NM_001127899.3:c.1016T>A
|
NP_001121371.1:p.Val339Asp
|
|
NM_001282163.1:c.866T>A
|
NP_001269092.1:p.Val289Asp
|
|
XM_011543888.1:c.1016T>A
|
XP_011542190.1:p.Val339Asp
|
|
XM_011543889.1:c.806T>A
|
XP_011542191.1:p.Val269Asp
|
|
XM_017029257.1:c.1028T>A
|
XP_016884746.1:p.Val343Asp
|
|
XM_017029258.1:c.1028T>A
|
XP_016884747.1:p.Val343Asp
|
|
NM_001127898.4:c.1016T>A
MANE Select
|
NP_001121370.1:p.Val339Asp
|
|
NM_000084.5:c.806T>A
|
NP_000075.1:p.Val269Asp
|
|
NM_001127899.4:c.1016T>A
|
NP_001121371.1:p.Val339Asp
|
|
NM_001282163.2:c.866T>A
|
NP_001269092.1:p.Val289Asp
|
|