ENST00000470050.2:c.1390G>T
|
ENSP00000515580.1:p.Ala464Ser
|
|
ENST00000703945.1:c.1306G>T
|
ENSP00000515578.1:p.Ala436Ser
|
|
ENST00000703946.1:c.1265+2516G>T
|
ENSP00000515579.1:n.1265+2516G>T
|
|
ENST00000703947.1:c.1000G>T
|
ENSP00000515581.1:p.Ala334Ser
|
|
ENST00000703948.1:c.*1007G>T
|
ENSP00000515582.1:n.*1007G>T
|
|
ENST00000703949.1:c.1390G>T
|
ENSP00000515583.1:p.Ala464Ser
|
|
ENST00000703950.1:c.1390G>T
|
ENSP00000515584.1:p.Ala464Ser
|
|
ENST00000703951.1:c.1265+2516G>T
|
ENSP00000515585.1:n.1265+2516G>T
|
|
ENST00000703952.1:c.1265+2516G>T
|
ENSP00000515586.1:n.1265+2516G>T
|
|
ENST00000703953.1:c.*653G>T
|
ENSP00000515587.1:n.*653G>T
|
|
ENST00000703954.1:c.1270G>T
|
ENSP00000515588.1:p.Ala424Ser
|
|
ENST00000703955.1:n.1940G>T
|
|
|
ENST00000298649.8:c.1387G>T
|
ENSP00000298649.3:p.Ala463Ser
|
|
ENST00000359426.7:c.1390G>T
MANE Select
|
ENSP00000352398.6:p.Ala464Ser
|
|
ENST00000436817.6:c.1402G>T
|
ENSP00000415949.2:p.Ala468Ser
|
|
ENST00000493591.6:c.*1278G>T
|
ENSP00000494917.1:n.*1278G>T
|
|
ENST00000643399.2:c.1402G>T
MANE Plus Clinical
|
ENSP00000494664.1:p.Ala468Ser
|
|
ENST00000298649.7:c.1387G>T
|
ENSP00000298649.3:p.Ala463Ser
|
|
ENST00000359426.6:c.1390G>T
|
ENSP00000352398.6:p.Ala464Ser
|
|
ENST00000360289.6:c.1354G>T
|
ENSP00000353433.2:p.Ala452Ser
|
|
ENST00000448642.6:c.1402G>T
|
ENSP00000402103.3:p.Ala468Ser
|
|
ENST00000494253.1:n.1616G>T
|
|
|
NM_000188.2:c.1390G>T
|
NP_000179.2:p.Ala464Ser
|
|
NM_033496.2:c.1387G>T
|
NP_277031.1:p.Ala463Ser
|
|
NM_033497.2:c.1402G>T
|
NP_277032.1:p.Ala468Ser
|
|
NM_033498.2:c.1402G>T
|
NP_277033.1:p.Ala468Ser
|
|
NM_033500.2:c.1354G>T , LRG_365t1:c.1354G>T
|
NP_277035.2:p.Ala452Ser
|
|
XM_005269735.2:c.1519G>T
|
XP_005269792.1:p.Ala507Ser
|
|
XM_005269736.1:c.1402G>T
|
XP_005269793.1:p.Ala468Ser
|
|
XM_005269737.1:c.1306G>T
|
XP_005269794.1:p.Ala436Ser
|
|
XM_011539732.1:c.1354G>T
|
XP_011538034.1:p.Ala452Ser
|
|
XM_011539733.1:c.1348G>T
|
XP_011538035.1:p.Ala450Ser
|
|
XM_011539734.1:c.1345G>T
|
XP_011538036.1:p.Ala449Ser
|
|
NM_001322364.1:c.1402G>T
|
NP_001309293.1:p.Ala468Ser
|
|
NM_001322365.1:c.1495G>T
|
NP_001309294.1:p.Ala499Ser
|
|
NM_001322366.1:c.1306G>T
|
NP_001309295.1:p.Ala436Ser
|
|
NM_001322367.1:c.1294G>T
|
NP_001309296.1:p.Ala432Ser
|
|
NM_001358263.1:c.1402G>T
MANE Plus Clinical
|
NP_001345192.1:p.Ala468Ser
|
|
XM_024447969.1:c.1402G>T
|
XP_024303737.1:p.Ala468Ser
|
|
NM_000188.3:c.1390G>T
MANE Select
|
NP_000179.2:p.Ala464Ser
|
|
NM_001322364.2:c.1402G>T
|
NP_001309293.1:p.Ala468Ser
|
|
NM_001322365.2:c.1495G>T
|
NP_001309294.1:p.Ala499Ser
|
|
NM_033496.3:c.1387G>T
|
NP_277031.1:p.Ala463Ser
|
|
NM_033497.3:c.1402G>T
|
NP_277032.1:p.Ala468Ser
|
|
NM_033498.3:c.1402G>T
|
NP_277033.1:p.Ala468Ser
|
|