ENST00000371757.7:c.3562A>T
MANE Select
|
ENSP00000360822.2:p.Thr1188Ser
|
|
ENST00000674572.1:c.3466A>T
|
ENSP00000501742.1:p.Thr1156Ser
|
|
ENST00000675090.1:c.3310A>T
|
ENSP00000501833.1:p.Thr1104Ser
|
|
ENST00000675399.1:c.3373A>T
|
ENSP00000501932.1:p.Thr1125Ser
|
|
ENST00000676421.1:c.3382A>T
|
ENSP00000502322.1:p.Thr1128Ser
|
|
ENST00000263604.5:c.3526A>T
|
ENSP00000263604.4:p.Thr1176Ser
|
|
ENST00000371757.6:c.3562A>T
|
ENSP00000360822.2:p.Thr1188Ser
|
|
ENST00000460750.5:c.*3235A>T
|
ENSP00000418777.1:n.*3235A>T
|
|
ENST00000475008.1:n.2868A>T
|
|
|
ENST00000486577.6:c.3508A>T
|
ENSP00000417578.3:p.Thr1170Ser
|
|
ENST00000487664.5:c.3625A>T
|
ENSP00000417851.2:p.Thr1209Ser
|
|
ENST00000488444.6:c.3547A>T
|
ENSP00000419007.3:p.Thr1183Ser
|
|
ENST00000490355.6:c.3562A>T
|
ENSP00000418003.3:p.Thr1188Ser
|
|
ENST00000491806.6:c.3505A>T
|
ENSP00000419086.3:p.Thr1169Ser
|
|
ENST00000628528.2:c.3490A>T
|
ENSP00000486374.1:p.Thr1164Ser
|
|
ENST00000630792.2:c.3460A>T
|
ENSP00000486486.1:p.Thr1154Ser
|
|
ENST00000631073.2:c.3568A>T
|
ENSP00000486130.1:p.Thr1190Ser
|
|
NM_001272003.1:c.3490A>T
|
NP_001258932.1:p.Thr1164Ser
|
|
NM_020822.2:c.3562A>T
|
NP_065873.2:p.Thr1188Ser
|
|
XM_011518877.1:c.3760A>T
|
XP_011517179.1:p.Thr1254Ser
|
|
XM_011518878.1:c.3706A>T
|
XP_011517180.1:p.Thr1236Ser
|
|
XM_011518879.1:c.3697A>T
|
XP_011517181.1:p.Thr1233Ser
|
|
XM_011518880.1:c.3526A>T
|
XP_011517182.1:p.Thr1176Ser
|
|
XM_011518881.1:c.3115A>T
|
XP_011517183.1:p.Thr1039Ser
|
|
XM_011518877.3:c.3760A>T
|
XP_011517179.1:p.Thr1254Ser
|
|
XM_011518878.3:c.3706A>T
|
XP_011517180.1:p.Thr1236Ser
|
|
XM_011518879.3:c.3697A>T
|
XP_011517181.1:p.Thr1233Ser
|
|
XM_011518881.3:c.3115A>T
|
XP_011517183.1:p.Thr1039Ser
|
|
XM_017014931.1:c.3559A>T
|
XP_016870420.1:p.Thr1187Ser
|
|
XM_017014932.1:c.3382A>T
|
XP_016870421.1:p.Thr1128Ser
|
|
XM_017014933.1:c.3115A>T
|
XP_016870422.1:p.Thr1039Ser
|
|
XM_024447617.1:c.3115A>T
|
XP_024303385.1:p.Thr1039Ser
|
|
XM_024447618.1:c.3115A>T
|
XP_024303386.1:p.Thr1039Ser
|
|
NM_020822.3:c.3562A>T
MANE Select
|
NP_065873.2:p.Thr1188Ser
|
|
NM_001272003.2:c.3490A>T
|
NP_001258932.1:p.Thr1164Ser
|
|