ENST00000350026.11:c.4598A>T
|
ENSP00000055163.8:p.Asn1533Ile
|
|
ENST00000414678.8:c.4667A>T
|
ENSP00000412835.3:p.Asn1556Ile
|
|
ENST00000637015.2:c.4886A>T
|
ENSP00000489729.2:p.Asn1629Ile
|
|
ENST00000346085.10:c.4637A>T
|
ENSP00000344546.5:p.Asn1546Ile
|
|
ENST00000350026.10:c.4349A>T
|
ENSP00000055163.7:p.Asn1450Ile
|
|
ENST00000414678.7:c.2915A>T
|
ENSP00000412835.2:p.Asn972Ile
|
|
ENST00000635849.1:c.2078A>T
|
ENSP00000490948.1:p.Asn693Ile
|
|
ENST00000635957.1:c.1709A>T
|
ENSP00000490385.1:p.Asn570Ile
|
|
ENST00000636227.1:n.3220A>T
|
|
|
ENST00000636254.1:n.677A>T
|
|
|
ENST00000636930.2:c.4757A>T
MANE Select
|
ENSP00000490491.2:p.Asn1586Ile
|
|
ENST00000636940.1:n.2754A>T
|
|
|
ENST00000637015.1:c.2125A>T
|
|
|
ENST00000637568.1:c.2039A>T
|
|
|
ENST00000637741.1:n.1423A>T
|
|
|
ENST00000637810.1:c.2099A>T
|
ENSP00000489636.1:p.Asn700Ile
|
|
ENST00000637904.1:c.2258A>T
|
ENSP00000490550.1:p.Asn753Ile
|
|
ENST00000647938.1:c.4388A>T
|
ENSP00000498155.1:p.Asn1463Ile
|
|
ENST00000346085.9:c.4388A>T
|
ENSP00000344546.4:p.Asn1463Ile
|
|
ENST00000350026.9:c.4349A>T
|
ENSP00000055163.7:p.Asn1450Ile
|
|
ENST00000414678.6:c.2915A>T
|
ENSP00000412835.2:p.Asn972Ile
|
|
NM_017519.2:c.4349A>T
|
NP_059989.2:p.Asn1450Ile
|
|
NM_020732.3:c.4388A>T
|
NP_065783.3:p.Asn1463Ile
|
|
XM_005267069.3:c.4508A>T
|
XP_005267126.2:p.Asn1503Ile
|
|
XM_011535984.1:c.3587A>T
|
XP_011534286.1:p.Asn1196Ile
|
|
XM_011535985.1:c.3407A>T
|
XP_011534287.1:p.Asn1136Ile
|
|
XM_011535986.1:c.3167A>T
|
XP_011534288.1:p.Asn1056Ile
|
|
XM_011535987.1:c.2786A>T
|
XP_011534289.1:p.Asn929Ile
|
|
XM_011535988.1:c.1649A>T
|
XP_011534290.1:p.Asn550Ile
|
|
NM_001346813.1:c.4508A>T
|
NP_001333742.1:p.Asn1503Ile
|
|
NM_001363725.1:c.2258A>T
|
NP_001350654.1:p.Asn753Ile
|
|
XM_011535984.2:c.4718A>T
|
XP_011534286.2:p.Asn1573Ile
|
|
XM_011535988.3:c.1649A>T
|
XP_011534290.1:p.Asn550Ile
|
|
XM_017011103.2:c.4619A>T
|
XP_016866592.1:p.Asn1540Ile
|
|
XM_017011104.1:c.4589A>T
|
XP_016866593.1:p.Asn1530Ile
|
|
XM_017011105.2:c.4559A>T
|
XP_016866594.1:p.Asn1520Ile
|
|
XM_017011106.2:c.4430A>T
|
XP_016866595.1:p.Asn1477Ile
|
|
XM_017011107.2:c.4409A>T
|
XP_016866596.1:p.Asn1470Ile
|
|
XR_002956289.1:n.4704A>T
|
|
|
NM_001363725.2:c.2258A>T
|
NP_001350654.1:p.Asn753Ile
|
|
NM_001371656.1:c.4637A>T
|
NP_001358585.1:p.Asn1546Ile
|
|
NM_001374820.1:c.4637A>T
|
NP_001361749.1:p.Asn1546Ile
|
|
NM_001374828.1:c.4757A>T
MANE Select
|
NP_001361757.1:p.Asn1586Ile
|
|
NM_017519.3:c.4598A>T
|
NP_059989.3:p.Asn1533Ile
|
|