ENST00000350026.11:c.3764A>C
|
ENSP00000055163.8:p.Asn1255Thr
|
|
ENST00000414678.8:c.3833A>C
|
ENSP00000412835.3:p.Asn1278Thr
|
|
ENST00000637015.2:c.4052A>C
|
ENSP00000489729.2:p.Asn1351Thr
|
|
ENST00000346085.10:c.3803A>C
|
ENSP00000344546.5:p.Asn1268Thr
|
|
ENST00000350026.10:c.3515A>C
|
ENSP00000055163.7:p.Asn1172Thr
|
|
ENST00000414678.7:c.2081A>C
|
ENSP00000412835.2:p.Asn694Thr
|
|
ENST00000635849.1:c.1244A>C
|
ENSP00000490948.1:p.Asn415Thr
|
|
ENST00000635957.1:c.878A>C
|
ENSP00000490385.1:p.Asn293Thr
|
|
ENST00000636930.2:c.3923A>C
MANE Select
|
ENSP00000490491.2:p.Asn1308Thr
|
|
ENST00000636940.1:n.1920A>C
|
|
|
ENST00000637015.1:c.1291A>C
|
|
|
ENST00000637568.1:c.1205A>C
|
|
|
ENST00000637741.1:n.589A>C
|
|
|
ENST00000637810.1:c.1265A>C
|
ENSP00000489636.1:p.Asn422Thr
|
|
ENST00000637904.1:c.1424A>C
|
ENSP00000490550.1:p.Asn475Thr
|
|
ENST00000647938.1:c.3554A>C
|
ENSP00000498155.1:p.Asn1185Thr
|
|
ENST00000346085.9:c.3554A>C
|
ENSP00000344546.4:p.Asn1185Thr
|
|
ENST00000350026.9:c.3515A>C
|
ENSP00000055163.7:p.Asn1172Thr
|
|
ENST00000414678.6:c.2081A>C
|
ENSP00000412835.2:p.Asn694Thr
|
|
NM_017519.2:c.3515A>C
|
NP_059989.2:p.Asn1172Thr
|
|
NM_020732.3:c.3554A>C
|
NP_065783.3:p.Asn1185Thr
|
|
XM_005267069.3:c.3674A>C
|
XP_005267126.2:p.Asn1225Thr
|
|
XM_011535984.1:c.2753A>C
|
XP_011534286.1:p.Asn918Thr
|
|
XM_011535985.1:c.2573A>C
|
XP_011534287.1:p.Asn858Thr
|
|
XM_011535986.1:c.2333A>C
|
XP_011534288.1:p.Asn778Thr
|
|
XM_011535987.1:c.1952A>C
|
XP_011534289.1:p.Asn651Thr
|
|
XM_011535988.1:c.815A>C
|
XP_011534290.1:p.Asn272Thr
|
|
NM_001346813.1:c.3674A>C
|
NP_001333742.1:p.Asn1225Thr
|
|
NM_001363725.1:c.1424A>C
|
NP_001350654.1:p.Asn475Thr
|
|
XM_011535984.2:c.3884A>C
|
XP_011534286.2:p.Asn1295Thr
|
|
XM_011535988.3:c.815A>C
|
XP_011534290.1:p.Asn272Thr
|
|
XM_017011103.2:c.3785A>C
|
XP_016866592.1:p.Asn1262Thr
|
|
XM_017011104.1:c.3755A>C
|
XP_016866593.1:p.Asn1252Thr
|
|
XM_017011105.2:c.3725A>C
|
XP_016866594.1:p.Asn1242Thr
|
|
XM_017011106.2:c.3596A>C
|
XP_016866595.1:p.Asn1199Thr
|
|
XM_017011107.2:c.3575A>C
|
XP_016866596.1:p.Asn1192Thr
|
|
XR_002956289.1:n.3967A>C
|
|
|
NM_001363725.2:c.1424A>C
|
NP_001350654.1:p.Asn475Thr
|
|
NM_001371656.1:c.3803A>C
|
NP_001358585.1:p.Asn1268Thr
|
|
NM_001374820.1:c.3803A>C
|
NP_001361749.1:p.Asn1268Thr
|
|
NM_001374828.1:c.3923A>C
MANE Select
|
NP_001361757.1:p.Asn1308Thr
|
|
NM_017519.3:c.3764A>C
|
NP_059989.3:p.Asn1255Thr
|
|