ENST00000553893.6:c.*2178T>A
|
ENSP00000452467.1:n.*2178T>A
|
|
ENST00000554327.6:c.1225T>A
|
|
|
ENST00000557058.2:n.1969T>A
|
|
|
ENST00000557257.2:c.2080T>A
|
ENSP00000450578.2:p.Ser694Thr
|
|
ENST00000557555.3:c.2566T>A
|
ENSP00000451039.3:p.Ser856Thr
|
|
ENST00000686981.1:c.*2265T>A
|
ENSP00000510795.1:n.*2265T>A
|
|
ENST00000687390.1:n.660T>A
|
|
|
ENST00000691052.1:c.*1038T>A
|
ENSP00000508886.1:n.*1038T>A
|
|
ENST00000691846.1:c.1367T>A
|
|
|
ENST00000691973.1:c.2566T>A
|
ENSP00000509141.1:p.Ser856Thr
|
|
ENST00000257879.11:c.2554T>A
MANE Select
|
ENSP00000257879.7:p.Ser852Thr
|
|
ENST00000553804.6:c.2566T>A
|
ENSP00000452120.1:p.Ser856Thr
|
|
ENST00000257879.10:c.2554T>A
|
ENSP00000257879.6:p.Ser852Thr
|
|
ENST00000347027.10:c.2536T>A
|
ENSP00000343009.6:p.Ser846Thr
|
|
ENST00000452168.6:c.2275T>A
|
ENSP00000393844.2:p.Ser759Thr
|
|
ENST00000553804.5:c.2566T>A
|
ENSP00000452120.1:p.Ser856Thr
|
|
ENST00000554327.5:c.619T>A
|
|
|
ENST00000555728.5:c.2686T>A
|
ENSP00000452387.1:p.Ser896Thr
|
|
NM_001144996.1:c.2566T>A
|
NP_001138468.1:p.Ser856Thr
|
|
NM_001144997.1:c.2275T>A
|
NP_001138469.1:p.Ser759Thr
|
|
NM_002206.2:c.2554T>A
|
NP_002197.2:p.Ser852Thr
|
|
XM_005268839.1:c.2686T>A
|
XP_005268896.1:p.Ser896Thr
|
|
XM_005268840.1:c.2668T>A
|
XP_005268897.1:p.Ser890Thr
|
|
XM_005268841.1:c.2686T>A
|
XP_005268898.1:p.Ser896Thr
|
|
XM_005268842.1:c.2536T>A
|
XP_005268899.1:p.Ser846Thr
|
|
XM_005268844.1:c.2347T>A
|
XP_005268901.1:p.Ser783Thr
|
|
XM_005268845.1:c.2215T>A
|
XP_005268902.1:p.Ser739Thr
|
|
XM_005268846.1:c.2215T>A
|
XP_005268903.1:p.Ser739Thr
|
|
XM_005268847.1:c.2212T>A
|
XP_005268904.1:p.Ser738Thr
|
|
XM_005268848.1:c.2212T>A
|
XP_005268905.1:p.Ser738Thr
|
|
XM_005268849.1:c.2212T>A
|
XP_005268906.1:p.Ser738Thr
|
|
XM_005268850.1:c.2080T>A
|
XP_005268907.1:p.Ser694Thr
|
|
XM_011538286.1:c.2347T>A
|
XP_011536588.1:p.Ser783Thr
|
|
XM_005268839.2:c.2686T>A
|
XP_005268896.1:p.Ser896Thr
|
|
XM_005268840.2:c.2668T>A
|
XP_005268897.1:p.Ser890Thr
|
|
XM_005268841.2:c.2686T>A
|
XP_005268898.1:p.Ser896Thr
|
|
XM_005268842.2:c.2536T>A
|
XP_005268899.1:p.Ser846Thr
|
|
XM_017019265.1:c.2296T>A
|
XP_016874754.1:p.Ser766Thr
|
|
NM_001144996.2:c.2566T>A
|
NP_001138468.1:p.Ser856Thr
|
|
NM_001367993.1:c.2227T>A
|
NP_001354922.1:p.Ser743Thr
|
|
NM_001367994.1:c.1210T>A
|
NP_001354923.1:p.Ser404Thr
|
|
NM_001374465.1:c.2536T>A
|
NP_001361394.1:p.Ser846Thr
|
|
NM_002206.3:c.2554T>A
MANE Select
|
NP_002197.2:p.Ser852Thr
|
|