ENST00000470050.2:c.1295G>C
|
ENSP00000515580.1:p.Arg432Thr
|
|
ENST00000703945.1:c.1211G>C
|
ENSP00000515578.1:p.Arg404Thr
|
|
ENST00000703946.1:c.1265+2421G>C
|
ENSP00000515579.1:n.1265+2421G>C
|
|
ENST00000703947.1:c.905G>C
|
ENSP00000515581.1:p.Arg302Thr
|
|
ENST00000703948.1:c.*912G>C
|
ENSP00000515582.1:n.*912G>C
|
|
ENST00000703949.1:c.1295G>C
|
ENSP00000515583.1:p.Arg432Thr
|
|
ENST00000703950.1:c.1295G>C
|
ENSP00000515584.1:p.Arg432Thr
|
|
ENST00000703951.1:c.1265+2421G>C
|
ENSP00000515585.1:n.1265+2421G>C
|
|
ENST00000703952.1:c.1265+2421G>C
|
ENSP00000515586.1:n.1265+2421G>C
|
|
ENST00000703953.1:c.*558G>C
|
ENSP00000515587.1:n.*558G>C
|
|
ENST00000703954.1:c.1175G>C
|
ENSP00000515588.1:p.Arg392Thr
|
|
ENST00000703955.1:n.1845G>C
|
|
|
ENST00000298649.8:c.1292G>C
|
ENSP00000298649.3:p.Arg431Thr
|
|
ENST00000359426.7:c.1295G>C
MANE Select
|
ENSP00000352398.6:p.Arg432Thr
|
|
ENST00000436817.6:c.1307G>C
|
ENSP00000415949.2:p.Arg436Thr
|
|
ENST00000493591.6:c.*1183G>C
|
ENSP00000494917.1:n.*1183G>C
|
|
ENST00000643399.2:c.1307G>C
MANE Plus Clinical
|
ENSP00000494664.1:p.Arg436Thr
|
|
ENST00000298649.7:c.1292G>C
|
ENSP00000298649.3:p.Arg431Thr
|
|
ENST00000359426.6:c.1295G>C
|
ENSP00000352398.6:p.Arg432Thr
|
|
ENST00000360289.6:c.1259G>C
|
ENSP00000353433.2:p.Arg420Thr
|
|
ENST00000448642.6:c.1307G>C
|
ENSP00000402103.3:p.Arg436Thr
|
|
ENST00000494253.1:n.1521G>C
|
|
|
NM_000188.2:c.1295G>C
|
NP_000179.2:p.Arg432Thr
|
|
NM_033496.2:c.1292G>C
|
NP_277031.1:p.Arg431Thr
|
|
NM_033497.2:c.1307G>C
|
NP_277032.1:p.Arg436Thr
|
|
NM_033498.2:c.1307G>C
|
NP_277033.1:p.Arg436Thr
|
|
NM_033500.2:c.1259G>C , LRG_365t1:c.1259G>C
|
NP_277035.2:p.Arg420Thr
|
|
XM_005269735.2:c.1424G>C
|
XP_005269792.1:p.Arg475Thr
|
|
XM_005269736.1:c.1307G>C
|
XP_005269793.1:p.Arg436Thr
|
|
XM_005269737.1:c.1211G>C
|
XP_005269794.1:p.Arg404Thr
|
|
XM_011539732.1:c.1259G>C
|
XP_011538034.1:p.Arg420Thr
|
|
XM_011539733.1:c.1253G>C
|
XP_011538035.1:p.Arg418Thr
|
|
XM_011539734.1:c.1250G>C
|
XP_011538036.1:p.Arg417Thr
|
|
NM_001322364.1:c.1307G>C
|
NP_001309293.1:p.Arg436Thr
|
|
NM_001322365.1:c.1400G>C
|
NP_001309294.1:p.Arg467Thr
|
|
NM_001322366.1:c.1211G>C
|
NP_001309295.1:p.Arg404Thr
|
|
NM_001322367.1:c.1199G>C
|
NP_001309296.1:p.Arg400Thr
|
|
NM_001358263.1:c.1307G>C
MANE Plus Clinical
|
NP_001345192.1:p.Arg436Thr
|
|
XM_024447969.1:c.1307G>C
|
XP_024303737.1:p.Arg436Thr
|
|
NM_000188.3:c.1295G>C
MANE Select
|
NP_000179.2:p.Arg432Thr
|
|
NM_001322364.2:c.1307G>C
|
NP_001309293.1:p.Arg436Thr
|
|
NM_001322365.2:c.1400G>C
|
NP_001309294.1:p.Arg467Thr
|
|
NM_033496.3:c.1292G>C
|
NP_277031.1:p.Arg431Thr
|
|
NM_033497.3:c.1307G>C
|
NP_277032.1:p.Arg436Thr
|
|
NM_033498.3:c.1307G>C
|
NP_277033.1:p.Arg436Thr
|
|