ENST00000350026.11:c.3979A>C
|
ENSP00000055163.8:p.Asn1327His
|
|
ENST00000414678.8:c.4048A>C
|
ENSP00000412835.3:p.Asn1350His
|
|
ENST00000637015.2:c.4267A>C
|
ENSP00000489729.2:p.Asn1423His
|
|
ENST00000346085.10:c.4018A>C
|
ENSP00000344546.5:p.Asn1340His
|
|
ENST00000350026.10:c.3730A>C
|
ENSP00000055163.7:p.Asn1244His
|
|
ENST00000414678.7:c.2296A>C
|
ENSP00000412835.2:p.Asn766His
|
|
ENST00000635849.1:c.1459A>C
|
ENSP00000490948.1:p.Asn487His
|
|
ENST00000635957.1:c.1090A>C
|
ENSP00000490385.1:p.Asn364His
|
|
ENST00000636930.2:c.4138A>C
MANE Select
|
ENSP00000490491.2:p.Asn1380His
|
|
ENST00000636940.1:n.2135A>C
|
|
|
ENST00000637015.1:c.1506A>C
|
|
|
ENST00000637568.1:c.1420A>C
|
|
|
ENST00000637741.1:n.804A>C
|
|
|
ENST00000637810.1:c.1480A>C
|
ENSP00000489636.1:p.Asn494His
|
|
ENST00000637904.1:c.1639A>C
|
ENSP00000490550.1:p.Asn547His
|
|
ENST00000647938.1:c.3769A>C
|
ENSP00000498155.1:p.Asn1257His
|
|
ENST00000346085.9:c.3769A>C
|
ENSP00000344546.4:p.Asn1257His
|
|
ENST00000350026.9:c.3730A>C
|
ENSP00000055163.7:p.Asn1244His
|
|
ENST00000414678.6:c.2296A>C
|
ENSP00000412835.2:p.Asn766His
|
|
NM_017519.2:c.3730A>C
|
NP_059989.2:p.Asn1244His
|
|
NM_020732.3:c.3769A>C
|
NP_065783.3:p.Asn1257His
|
|
XM_005267069.3:c.3889A>C
|
XP_005267126.2:p.Asn1297His
|
|
XM_011535984.1:c.2968A>C
|
XP_011534286.1:p.Asn990His
|
|
XM_011535985.1:c.2788A>C
|
XP_011534287.1:p.Asn930His
|
|
XM_011535986.1:c.2548A>C
|
XP_011534288.1:p.Asn850His
|
|
XM_011535987.1:c.2167A>C
|
XP_011534289.1:p.Asn723His
|
|
XM_011535988.1:c.1030A>C
|
XP_011534290.1:p.Asn344His
|
|
NM_001346813.1:c.3889A>C
|
NP_001333742.1:p.Asn1297His
|
|
NM_001363725.1:c.1639A>C
|
NP_001350654.1:p.Asn547His
|
|
XM_011535984.2:c.4099A>C
|
XP_011534286.2:p.Asn1367His
|
|
XM_011535988.3:c.1030A>C
|
XP_011534290.1:p.Asn344His
|
|
XM_017011103.2:c.4000A>C
|
XP_016866592.1:p.Asn1334His
|
|
XM_017011104.1:c.3970A>C
|
XP_016866593.1:p.Asn1324His
|
|
XM_017011105.2:c.3940A>C
|
XP_016866594.1:p.Asn1314His
|
|
XM_017011106.2:c.3811A>C
|
XP_016866595.1:p.Asn1271His
|
|
XM_017011107.2:c.3790A>C
|
XP_016866596.1:p.Asn1264His
|
|
XR_002956289.1:n.4182A>C
|
|
|
NM_001363725.2:c.1639A>C
|
NP_001350654.1:p.Asn547His
|
|
NM_001371656.1:c.4018A>C
|
NP_001358585.1:p.Asn1340His
|
|
NM_001374820.1:c.4018A>C
|
NP_001361749.1:p.Asn1340His
|
|
NM_001374828.1:c.4138A>C
MANE Select
|
NP_001361757.1:p.Asn1380His
|
|
NM_017519.3:c.3979A>C
|
NP_059989.3:p.Asn1327His
|
|