|
ENST00000336425.10:c.980C>G
|
ENSP00000338087.7:p.Thr327Ser
|
|
|
ENST00000411653.6:c.980C>G
|
ENSP00000411326.3:p.Thr327Ser
|
|
|
ENST00000422328.6:c.*769C>G
|
ENSP00000415892.3:n.*769C>G
|
|
|
ENST00000448866.7:c.980C>G
MANE Select
|
ENSP00000402536.3:p.Thr327Ser
|
|
|
ENST00000458722.6:c.1118C>G
|
ENSP00000411274.3:p.Thr373Ser
|
|
|
ENST00000650822.1:c.983C>G
|
ENSP00000498517.1:p.Thr328Ser
|
|
|
ENST00000652056.1:c.983C>G
|
ENSP00000498271.1:p.Thr328Ser
|
|
|
ENST00000263552.10:c.983C>G
|
ENSP00000263552.6:p.Thr328Ser
|
|
|
ENST00000336425.9:c.980C>G
|
ENSP00000338087.5:p.Thr327Ser
|
|
|
ENST00000411653.5:c.980C>G
|
ENSP00000411326.1:p.Thr327Ser
|
|
|
ENST00000414508.6:c.983C>G
|
ENSP00000392702.2:p.Thr328Ser
|
|
|
ENST00000416849.6:c.1121C>G
|
ENSP00000389414.2:p.Thr374Ser
|
|
|
ENST00000422328.5:c.*769C>G
|
ENSP00000415892.1:n.*769C>G
|
|
|
ENST00000425687.5:c.779C>G
|
ENSP00000388736.1:p.Thr260Ser
|
|
|
ENST00000448866.5:c.980C>G
|
ENSP00000402536.1:p.Thr327Ser
|
|
|
ENST00000458722.5:c.1118C>G
|
ENSP00000411274.1:p.Thr373Ser
|
|
|
ENST00000462275.5:n.951C>G
|
|
|
|
ENST00000469630.1:n.463C>G
|
|
|
|
ENST00000494876.1:n.345C>G
|
|
|
|
NM_001061.4:c.983C>G
|
NP_001052.2:p.Thr328Ser
|
|
|
NM_001130966.2:c.983C>G , LRG_579t1:c.983C>G
|
NP_001124438.1:p.Thr328Ser
|
|
|
NM_001166253.1:c.1121C>G , LRG_579t4:c.1121C>G
|
NP_001159725.1:p.Thr374Ser
|
|
|
NM_001166254.1:c.779C>G , LRG_579t3:c.779C>G
|
NP_001159726.1:p.Thr260Ser
|
|
|
NM_001314028.1:c.923C>G
|
NP_001300957.1:p.Thr308Ser
|
|
|
NM_030984.3:c.983C>G , LRG_579t2:c.983C>G
|
NP_112246.2:p.Thr328Ser
|
|
|
NR_029394.1:c.-4294966049C>G
|
|
|
|
XM_011516544.1:c.983C>G
|
XP_011514846.1:p.Thr328Ser
|
|
|
NM_001061.5:c.980C>G
|
NP_001052.3:p.Thr327Ser
|
|
|
NM_001130966.3:c.980C>G
|
NP_001124438.2:p.Thr327Ser
|
|
|
NM_001166253.2:c.1118C>G
|
NP_001159725.2:p.Thr373Ser
|
|
|
NM_001166254.2:c.779C>G
|
NP_001159726.1:p.Thr260Ser
|
|
|
NM_001314028.2:c.923C>G
|
NP_001300957.1:p.Thr308Ser
|
|
|
NM_001366537.1:c.797C>G
|
NP_001353466.1:p.Thr266Ser
|
|
|
NM_030984.4:c.980C>G
|
NP_112246.3:p.Thr327Ser
|
|
|
XM_011516544.3:c.983C>G
|
XP_011514846.1:p.Thr328Ser
|
|
|
XM_017012570.2:c.983C>G
|
XP_016868059.1:p.Thr328Ser
|
|
|
XM_017012571.2:c.983C>G
|
XP_016868060.1:p.Thr328Ser
|
|
|
XM_017012572.2:c.983C>G
|
XP_016868061.1:p.Thr328Ser
|
|
|
XM_024446901.1:c.725C>G
|
XP_024302669.1:p.Thr242Ser
|
|
|
NM_001061.7:c.980C>G
MANE Select
|
NP_001052.3:p.Thr327Ser
|
|
|
NM_001130966.4:c.980C>G
|
NP_001124438.2:p.Thr327Ser
|
|
|
NM_001166253.3:c.1118C>G
|
NP_001159725.2:p.Thr373Ser
|
|
|
NM_001166254.3:c.779C>G
|
NP_001159726.1:p.Thr260Ser
|
|
|
NM_001314028.3:c.923C>G
|
NP_001300957.1:p.Thr308Ser
|
|
|
NM_001366537.2:c.797C>G
|
NP_001353466.1:p.Thr266Ser
|
|
|
NM_030984.5:c.980C>G
|
NP_112246.3:p.Thr327Ser
|
|
|
NM_001130966.5:c.980C>G
|
NP_001124438.2:p.Thr327Ser
|
|
|
NM_001166253.4:c.1118C>G
|
NP_001159725.2:p.Thr373Ser
|
|
|
NM_001166254.4:c.779C>G
|
NP_001159726.1:p.Thr260Ser
|
|
|
NM_001314028.4:c.923C>G
|
NP_001300957.1:p.Thr308Ser
|
|
|
NM_001366537.3:c.797C>G
|
NP_001353466.1:p.Thr266Ser
|
|
|
NM_030984.6:c.980C>G
|
NP_112246.3:p.Thr327Ser
|
|
