ENST00000350026.11:c.4985T>A
|
ENSP00000055163.8:p.Val1662Asp
|
|
ENST00000414678.8:c.5054T>A
|
ENSP00000412835.3:p.Val1685Asp
|
|
ENST00000637015.2:c.5273T>A
|
ENSP00000489729.2:p.Val1758Asp
|
|
ENST00000346085.10:c.5024T>A
|
ENSP00000344546.5:p.Val1675Asp
|
|
ENST00000350026.10:c.4736T>A
|
ENSP00000055163.7:p.Val1579Asp
|
|
ENST00000414678.7:c.3302T>A
|
ENSP00000412835.2:p.Val1101Asp
|
|
ENST00000635849.1:c.2465T>A
|
ENSP00000490948.1:p.Val822Asp
|
|
ENST00000635957.1:c.2096T>A
|
ENSP00000490385.1:p.Val699Asp
|
|
ENST00000636227.1:n.3607T>A
|
|
|
ENST00000636254.1:n.1064T>A
|
|
|
ENST00000636930.2:c.5144T>A
MANE Select
|
ENSP00000490491.2:p.Val1715Asp
|
|
ENST00000636940.1:n.3141T>A
|
|
|
ENST00000637015.1:c.2512T>A
|
|
|
ENST00000637568.1:c.2426T>A
|
|
|
ENST00000637741.1:n.1810T>A
|
|
|
ENST00000637810.1:c.2486T>A
|
ENSP00000489636.1:p.Val829Asp
|
|
ENST00000637904.1:c.2645T>A
|
ENSP00000490550.1:p.Val882Asp
|
|
ENST00000647938.1:c.4775T>A
|
ENSP00000498155.1:p.Val1592Asp
|
|
ENST00000346085.9:c.4775T>A
|
ENSP00000344546.4:p.Val1592Asp
|
|
ENST00000350026.9:c.4736T>A
|
ENSP00000055163.7:p.Val1579Asp
|
|
ENST00000414678.6:c.3302T>A
|
ENSP00000412835.2:p.Val1101Asp
|
|
NM_017519.2:c.4736T>A
|
NP_059989.2:p.Val1579Asp
|
|
NM_020732.3:c.4775T>A
|
NP_065783.3:p.Val1592Asp
|
|
XM_005267069.3:c.4895T>A
|
XP_005267126.2:p.Val1632Asp
|
|
XM_011535984.1:c.3974T>A
|
XP_011534286.1:p.Val1325Asp
|
|
XM_011535985.1:c.3794T>A
|
XP_011534287.1:p.Val1265Asp
|
|
XM_011535986.1:c.3554T>A
|
XP_011534288.1:p.Val1185Asp
|
|
XM_011535987.1:c.3173T>A
|
XP_011534289.1:p.Val1058Asp
|
|
XM_011535988.1:c.2036T>A
|
XP_011534290.1:p.Val679Asp
|
|
NM_001346813.1:c.4895T>A
|
NP_001333742.1:p.Val1632Asp
|
|
NM_001363725.1:c.2645T>A
|
NP_001350654.1:p.Val882Asp
|
|
XM_011535984.2:c.5105T>A
|
XP_011534286.2:p.Val1702Asp
|
|
XM_011535988.3:c.2036T>A
|
XP_011534290.1:p.Val679Asp
|
|
XM_017011103.2:c.5006T>A
|
XP_016866592.1:p.Val1669Asp
|
|
XM_017011104.1:c.4976T>A
|
XP_016866593.1:p.Val1659Asp
|
|
XM_017011105.2:c.4946T>A
|
XP_016866594.1:p.Val1649Asp
|
|
XM_017011106.2:c.4817T>A
|
XP_016866595.1:p.Val1606Asp
|
|
XM_017011107.2:c.4796T>A
|
XP_016866596.1:p.Val1599Asp
|
|
XR_002956289.1:n.5091T>A
|
|
|
NM_001363725.2:c.2645T>A
|
NP_001350654.1:p.Val882Asp
|
|
NM_001371656.1:c.5024T>A
|
NP_001358585.1:p.Val1675Asp
|
|
NM_001374820.1:c.5024T>A
|
NP_001361749.1:p.Val1675Asp
|
|
NM_001374828.1:c.5144T>A
MANE Select
|
NP_001361757.1:p.Val1715Asp
|
|
NM_017519.3:c.4985T>A
|
NP_059989.3:p.Val1662Asp
|
|