ENST00000350026.11:c.3047C>A
|
ENSP00000055163.8:p.Ala1016Asp
|
|
ENST00000414678.8:c.2957C>A
|
ENSP00000412835.3:p.Ala986Asp
|
|
ENST00000637015.2:c.3047C>A
|
ENSP00000489729.2:p.Ala1016Asp
|
|
ENST00000319584.11:c.1061C>A
|
ENSP00000313006.7:p.Ala354Asp
|
|
ENST00000346085.10:c.3086C>A
|
ENSP00000344546.5:p.Ala1029Asp
|
|
ENST00000350026.10:c.2798C>A
|
ENSP00000055163.7:p.Ala933Asp
|
|
ENST00000414678.7:c.1205C>A
|
ENSP00000412835.2:p.Ala402Asp
|
|
ENST00000452544.2:n.948C>A
|
|
|
ENST00000635849.1:c.368C>A
|
ENSP00000490948.1:p.Ala123Asp
|
|
ENST00000635957.1:c.2C>A
|
ENSP00000490385.1:p.Ala1Asp
|
|
ENST00000636426.1:n.181C>A
|
|
|
ENST00000636930.2:c.3047C>A
MANE Select
|
ENSP00000490491.2:p.Ala1016Asp
|
|
ENST00000637015.1:c.286C>A
|
|
|
ENST00000637568.1:c.90C>A
|
|
|
ENST00000637810.1:c.548C>A
|
ENSP00000489636.1:p.Ala183Asp
|
|
ENST00000637904.1:c.548C>A
|
ENSP00000490550.1:p.Ala183Asp
|
|
ENST00000647938.1:c.2837C>A
|
ENSP00000498155.1:p.Ala946Asp
|
|
ENST00000674190.1:n.1796C>A
|
|
|
ENST00000319584.10:c.1064C>A
|
ENSP00000313006.6:p.Ala355Asp
|
|
ENST00000346085.9:c.2837C>A
|
ENSP00000344546.4:p.Ala946Asp
|
|
ENST00000350026.9:c.2798C>A
|
ENSP00000055163.7:p.Ala933Asp
|
|
ENST00000414678.6:c.1205C>A
|
ENSP00000412835.2:p.Ala402Asp
|
|
ENST00000452544.1:n.894C>A
|
|
|
ENST00000478761.3:c.120C>A
|
|
|
NM_017519.2:c.2798C>A
|
NP_059989.2:p.Ala933Asp
|
|
NM_020732.3:c.2837C>A
|
NP_065783.3:p.Ala946Asp
|
|
XM_005267069.3:c.2798C>A
|
XP_005267126.2:p.Ala933Asp
|
|
XM_011535984.1:c.1748C>A
|
XP_011534286.1:p.Ala583Asp
|
|
XM_011535985.1:c.1568C>A
|
XP_011534287.1:p.Ala523Asp
|
|
XM_011535986.1:c.1328C>A
|
XP_011534288.1:p.Ala443Asp
|
|
XM_011535987.1:c.947C>A
|
XP_011534289.1:p.Ala316Asp
|
|
XM_011535988.1:c.-20+15702C>A
|
XP_011534290.1:n.-20+15702C>A
|
|
NM_001346813.1:c.2798C>A
|
NP_001333742.1:p.Ala933Asp
|
|
NM_001363725.1:c.548C>A
|
NP_001350654.1:p.Ala183Asp
|
|
XM_011535984.2:c.2879C>A
|
XP_011534286.2:p.Ala960Asp
|
|
XM_011535988.3:c.-20+15702C>A
|
XP_011534290.1:n.-20+15702C>A
|
|
XM_017011103.2:c.2879C>A
|
XP_016866592.1:p.Ala960Asp
|
|
XM_017011104.1:c.2879C>A
|
XP_016866593.1:p.Ala960Asp
|
|
XM_017011105.2:c.2879C>A
|
XP_016866594.1:p.Ala960Asp
|
|
XM_017011106.2:c.2879C>A
|
XP_016866595.1:p.Ala960Asp
|
|
XM_017011107.2:c.2699C>A
|
XP_016866596.1:p.Ala900Asp
|
|
XR_002956289.1:n.2962C>A
|
|
|
NM_001363725.2:c.548C>A
|
NP_001350654.1:p.Ala183Asp
|
|
NM_001371656.1:c.3086C>A
|
NP_001358585.1:p.Ala1029Asp
|
|
NM_001374820.1:c.3086C>A
|
NP_001361749.1:p.Ala1029Asp
|
|
NM_001374828.1:c.3047C>A
MANE Select
|
NP_001361757.1:p.Ala1016Asp
|
|
NM_017519.3:c.3047C>A
|
NP_059989.3:p.Ala1016Asp
|
|