ENST00000320185.7:c.329A>T
MANE Select
|
ENSP00000321797.2:p.Asp110Val
|
|
ENST00000618991.5:c.17A>T
|
ENSP00000484420.1:p.Asp6Val
|
|
ENST00000344255.8:c.296A>T
|
ENSP00000340039.3:p.Asp99Val
|
|
ENST00000320185.6:c.329A>T
|
ENSP00000321797.2:p.Asp110Val
|
|
ENST00000344255.7:c.296A>T
|
ENSP00000340039.3:p.Asp99Val
|
|
ENST00000346714.7:c.209A>T
|
ENSP00000344306.3:p.Asp70Val
|
|
ENST00000347978.2:c.242A>T
|
ENSP00000321945.2:p.Asp81Val
|
|
ENST00000469792.6:c.*293A>T
|
ENSP00000473299.1:n.*293A>T
|
|
ENST00000485728.1:n.205A>T
|
|
|
ENST00000618991.4:c.17A>T
|
ENSP00000484420.1:p.Asp6Val
|
|
NM_001206389.1:c.17A>T
|
NP_001193318.1:p.Asp6Val
|
|
NM_006119.4:c.242A>T
|
NP_006110.1:p.Asp81Val
|
|
NM_033163.3:c.329A>T
|
NP_149353.1:p.Asp110Val
|
|
NM_033164.3:c.296A>T
|
NP_149354.1:p.Asp99Val
|
|
NM_033165.3:c.209A>T
|
NP_149355.1:p.Asp70Val
|
|
XM_011539509.1:c.251A>T
|
XP_011537811.1:p.Asp84Val
|
|
NM_006119.5:c.242A>T
|
NP_006110.1:p.Asp81Val
|
|
NM_033163.4:c.329A>T
|
NP_149353.1:p.Asp110Val
|
|
NM_033164.4:c.296A>T
|
NP_149354.1:p.Asp99Val
|
|
NM_033165.4:c.209A>T
|
NP_149355.1:p.Asp70Val
|
|
NM_001206389.2:c.17A>T
|
NP_001193318.1:p.Asp6Val
|
|
NM_006119.6:c.242A>T
|
NP_006110.1:p.Asp81Val
|
|
NM_033163.5:c.329A>T
MANE Select
|
NP_149353.1:p.Asp110Val
|
|
NM_033165.5:c.209A>T
|
NP_149355.1:p.Asp70Val
|
|