ENST00000350026.11:c.2357C>A
|
ENSP00000055163.8:p.Ala786Glu
|
|
ENST00000414678.8:c.2357C>A
|
ENSP00000412835.3:p.Ala786Glu
|
|
ENST00000637015.2:c.2357C>A
|
ENSP00000489729.2:p.Ala786Glu
|
|
ENST00000319584.11:c.371C>A
|
ENSP00000313006.7:p.Ala124Glu
|
|
ENST00000346085.10:c.2396C>A
|
ENSP00000344546.5:p.Ala799Glu
|
|
ENST00000350026.10:c.2108C>A
|
ENSP00000055163.7:p.Ala703Glu
|
|
ENST00000414678.7:c.605C>A
|
ENSP00000412835.2:p.Ala202Glu
|
|
ENST00000452544.2:n.258C>A
|
|
|
ENST00000493658.2:n.6C>A
|
|
|
ENST00000635849.1:c.-143C>A
|
ENSP00000490948.1:n.-143C>A
|
|
ENST00000636930.2:c.2357C>A
MANE Select
|
ENSP00000490491.2:p.Ala786Glu
|
|
ENST00000637003.1:c.-143C>A
|
ENSP00000489666.1:n.-143C>A
|
|
ENST00000637904.1:c.-143C>A
|
ENSP00000490550.1:n.-143C>A
|
|
ENST00000647938.1:c.2147C>A
|
ENSP00000498155.1:p.Ala716Glu
|
|
ENST00000674190.1:n.1106C>A
|
|
|
ENST00000319584.10:c.374C>A
|
ENSP00000313006.6:p.Ala125Glu
|
|
ENST00000346085.9:c.2147C>A
|
ENSP00000344546.4:p.Ala716Glu
|
|
ENST00000350026.9:c.2108C>A
|
ENSP00000055163.7:p.Ala703Glu
|
|
ENST00000414678.6:c.605C>A
|
ENSP00000412835.2:p.Ala202Glu
|
|
ENST00000452544.1:n.216C>A
|
|
|
ENST00000493658.1:n.6C>A
|
|
|
NM_017519.2:c.2108C>A
|
NP_059989.2:p.Ala703Glu
|
|
NM_020732.3:c.2147C>A
|
NP_065783.3:p.Ala716Glu
|
|
XM_005267069.3:c.2108C>A
|
XP_005267126.2:p.Ala703Glu
|
|
XM_011535984.1:c.1058C>A
|
XP_011534286.1:p.Ala353Glu
|
|
XM_011535985.1:c.1058C>A
|
XP_011534287.1:p.Ala353Glu
|
|
XM_011535986.1:c.638C>A
|
XP_011534288.1:p.Ala213Glu
|
|
XM_011535987.1:c.257C>A
|
XP_011534289.1:p.Ala86Glu
|
|
NM_001346813.1:c.2108C>A
|
NP_001333742.1:p.Ala703Glu
|
|
NM_001363725.1:c.-143C>A
|
NP_001350654.1:n.-143C>A
|
|
XM_011535984.2:c.2189C>A
|
XP_011534286.2:p.Ala730Glu
|
|
XM_017011103.2:c.2189C>A
|
XP_016866592.1:p.Ala730Glu
|
|
XM_017011104.1:c.2189C>A
|
XP_016866593.1:p.Ala730Glu
|
|
XM_017011105.2:c.2189C>A
|
XP_016866594.1:p.Ala730Glu
|
|
XM_017011106.2:c.2189C>A
|
XP_016866595.1:p.Ala730Glu
|
|
XM_017011107.2:c.2189C>A
|
XP_016866596.1:p.Ala730Glu
|
|
XR_002956289.1:n.2272C>A
|
|
|
NM_001363725.2:c.-143C>A
|
NP_001350654.1:n.-143C>A
|
|
NM_001371656.1:c.2396C>A
|
NP_001358585.1:p.Ala799Glu
|
|
NM_001374820.1:c.2396C>A
|
NP_001361749.1:p.Ala799Glu
|
|
NM_001374828.1:c.2357C>A
MANE Select
|
NP_001361757.1:p.Ala786Glu
|
|
NM_017519.3:c.2357C>A
|
NP_059989.3:p.Ala786Glu
|
|