ENST00000350026.11:c.3965A>C
|
ENSP00000055163.8:p.Asn1322Thr
|
|
ENST00000414678.8:c.4034A>C
|
ENSP00000412835.3:p.Asn1345Thr
|
|
ENST00000637015.2:c.4253A>C
|
ENSP00000489729.2:p.Asn1418Thr
|
|
ENST00000346085.10:c.4004A>C
|
ENSP00000344546.5:p.Asn1335Thr
|
|
ENST00000350026.10:c.3716A>C
|
ENSP00000055163.7:p.Asn1239Thr
|
|
ENST00000414678.7:c.2282A>C
|
ENSP00000412835.2:p.Asn761Thr
|
|
ENST00000635849.1:c.1445A>C
|
ENSP00000490948.1:p.Asn482Thr
|
|
ENST00000635957.1:c.1076A>C
|
ENSP00000490385.1:p.Asn359Thr
|
|
ENST00000636930.2:c.4124A>C
MANE Select
|
ENSP00000490491.2:p.Asn1375Thr
|
|
ENST00000636940.1:n.2121A>C
|
|
|
ENST00000637015.1:c.1492A>C
|
|
|
ENST00000637568.1:c.1406A>C
|
|
|
ENST00000637741.1:n.790A>C
|
|
|
ENST00000637810.1:c.1466A>C
|
ENSP00000489636.1:p.Asn489Thr
|
|
ENST00000637904.1:c.1625A>C
|
ENSP00000490550.1:p.Asn542Thr
|
|
ENST00000647938.1:c.3755A>C
|
ENSP00000498155.1:p.Asn1252Thr
|
|
ENST00000346085.9:c.3755A>C
|
ENSP00000344546.4:p.Asn1252Thr
|
|
ENST00000350026.9:c.3716A>C
|
ENSP00000055163.7:p.Asn1239Thr
|
|
ENST00000414678.6:c.2282A>C
|
ENSP00000412835.2:p.Asn761Thr
|
|
NM_017519.2:c.3716A>C
|
NP_059989.2:p.Asn1239Thr
|
|
NM_020732.3:c.3755A>C
|
NP_065783.3:p.Asn1252Thr
|
|
XM_005267069.3:c.3875A>C
|
XP_005267126.2:p.Asn1292Thr
|
|
XM_011535984.1:c.2954A>C
|
XP_011534286.1:p.Asn985Thr
|
|
XM_011535985.1:c.2774A>C
|
XP_011534287.1:p.Asn925Thr
|
|
XM_011535986.1:c.2534A>C
|
XP_011534288.1:p.Asn845Thr
|
|
XM_011535987.1:c.2153A>C
|
XP_011534289.1:p.Asn718Thr
|
|
XM_011535988.1:c.1016A>C
|
XP_011534290.1:p.Asn339Thr
|
|
NM_001346813.1:c.3875A>C
|
NP_001333742.1:p.Asn1292Thr
|
|
NM_001363725.1:c.1625A>C
|
NP_001350654.1:p.Asn542Thr
|
|
XM_011535984.2:c.4085A>C
|
XP_011534286.2:p.Asn1362Thr
|
|
XM_011535988.3:c.1016A>C
|
XP_011534290.1:p.Asn339Thr
|
|
XM_017011103.2:c.3986A>C
|
XP_016866592.1:p.Asn1329Thr
|
|
XM_017011104.1:c.3956A>C
|
XP_016866593.1:p.Asn1319Thr
|
|
XM_017011105.2:c.3926A>C
|
XP_016866594.1:p.Asn1309Thr
|
|
XM_017011106.2:c.3797A>C
|
XP_016866595.1:p.Asn1266Thr
|
|
XM_017011107.2:c.3776A>C
|
XP_016866596.1:p.Asn1259Thr
|
|
XR_002956289.1:n.4168A>C
|
|
|
NM_001363725.2:c.1625A>C
|
NP_001350654.1:p.Asn542Thr
|
|
NM_001371656.1:c.4004A>C
|
NP_001358585.1:p.Asn1335Thr
|
|
NM_001374820.1:c.4004A>C
|
NP_001361749.1:p.Asn1335Thr
|
|
NM_001374828.1:c.4124A>C
MANE Select
|
NP_001361757.1:p.Asn1375Thr
|
|
NM_017519.3:c.3965A>C
|
NP_059989.3:p.Asn1322Thr
|
|