|
ENST00000377313.7:c.1670C>G
|
ENSP00000366530.1:p.Thr557Ser
|
|
|
ENST00000394374.8:c.*963C>G
|
ENSP00000377899.4:n.*963C>G
|
|
|
ENST00000394376.7:c.1646C>G
|
ENSP00000377901.3:p.Thr549Ser
|
|
|
ENST00000413626.2:c.1655C>G
|
ENSP00000411218.2:p.Thr552Ser
|
|
|
ENST00000424912.2:c.1655C>G
|
ENSP00000388016.2:p.Thr552Ser
|
|
|
ENST00000429702.6:c.1655C>G
|
ENSP00000402752.2:p.Thr552Ser
|
|
|
ENST00000672079.2:c.*751C>G
|
ENSP00000500905.2:n.*751C>G
|
|
|
ENST00000710881.1:c.1670C>G
|
ENSP00000518530.1:p.Thr557Ser
|
|
|
ENST00000394376.6:c.997C>G
|
|
|
|
ENST00000478548.3:n.2148C>G
|
|
|
|
ENST00000671939.2:n.1617C>G
|
|
|
|
ENST00000671965.2:n.2037C>G
|
|
|
|
ENST00000312049.11:c.1655C>G
|
ENSP00000308975.6:p.Thr552Ser
|
|
|
ENST00000315422.9:c.1655C>G
|
ENSP00000323747.4:p.Thr552Ser
|
|
|
ENST00000377313.6:c.1670C>G
|
ENSP00000366530.1:p.Thr557Ser
|
|
|
ENST00000440873.6:c.1655C>G
|
ENSP00000413944.2:p.Thr552Ser
|
|
|
ENST00000450708.7:c.1655C>G
MANE Select
|
ENSP00000394933.3:p.Thr552Ser
|
|
|
ENST00000478548.2:n.2156C>G
|
|
|
|
ENST00000671939.1:n.1932C>G
|
|
|
|
ENST00000672304.1:c.1781C>G
|
ENSP00000500585.1:p.Thr594Ser
|
|
|
ENST00000312049.10:c.1655C>G
|
ENSP00000308975.6:p.Thr552Ser
|
|
|
ENST00000315422.8:c.1655C>G
|
ENSP00000323747.4:p.Thr552Ser
|
|
|
ENST00000337652.5:c.1670C>G
|
ENSP00000337088.1:p.Thr557Ser
|
|
|
ENST00000377313.5:c.1670C>G
|
ENSP00000366530.1:p.Thr557Ser
|
|
|
ENST00000377316.6:c.1490C>G
|
ENSP00000366533.1:p.Thr497Ser
|
|
|
ENST00000377321.5:c.1550C>G
|
ENSP00000366538.1:p.Thr517Ser
|
|
|
ENST00000377326.7:c.1655C>G
|
ENSP00000366543.3:p.Thr552Ser
|
|
|
ENST00000394374.6:c.1670C>G
|
ENSP00000377899.2:p.Thr557Ser
|
|
|
ENST00000394376.5:c.1670C>G
|
ENSP00000377901.1:p.Thr557Ser
|
|
|
ENST00000478548.1:n.1204C>G
|
|
|
|
NM_000244.3:c.1670C>G , LRG_509t1:c.1670C>G
|
NP_000235.2:p.Thr557Ser
|
|
|
NM_130799.2:c.1655C>G , LRG_509t2:c.1655C>G
|
NP_570711.1:p.Thr552Ser
|
|
|
NM_130800.2:c.1670C>G
|
NP_570712.1:p.Thr557Ser
|
|
|
NM_130801.2:c.1670C>G
|
NP_570713.1:p.Thr557Ser
|
|
|
NM_130802.2:c.1670C>G
|
NP_570714.1:p.Thr557Ser
|
|
|
NM_130803.2:c.1670C>G
|
NP_570715.1:p.Thr557Ser
|
|
|
NM_130804.2:c.1670C>G
|
NP_570716.1:p.Thr557Ser
|
|
|
XM_005274001.3:c.1655C>G
|
XP_005274058.1:p.Thr552Ser
|
|
|
XM_011545040.1:c.1781C>G
|
XP_011543342.1:p.Thr594Ser
|
|
|
XM_011545041.1:c.1781C>G
|
XP_011543343.1:p.Thr594Ser
|
|
|
XM_011545042.1:c.1781C>G
|
XP_011543344.1:p.Thr594Ser
|
|
|
XM_005274001.4:c.1655C>G
|
XP_005274058.1:p.Thr552Ser
|
|
|
XM_011545041.2:c.1781C>G
|
XP_011543343.1:p.Thr594Ser
|
|
|
XM_011545042.3:c.1781C>G
|
XP_011543344.1:p.Thr594Ser
|
|
|
XM_017017765.1:c.1796C>G
|
XP_016873254.1:p.Thr599Ser
|
|
|
XM_017017766.1:c.1796C>G
|
XP_016873255.1:p.Thr599Ser
|
|
|
XM_017017767.2:c.1796C>G
|
XP_016873256.1:p.Thr599Ser
|
|
|
XM_017017768.1:c.1796C>G
|
XP_016873257.1:p.Thr599Ser
|
|
|
XM_017017769.1:c.1655C>G
|
XP_016873258.1:p.Thr552Ser
|
|
|
XM_017017770.2:c.1655C>G
|
XP_016873259.1:p.Thr552Ser
|
|
|
NM_001370251.1:c.1781C>G
|
NP_001357180.1:p.Thr594Ser
|
|
|
NM_001370259.2:c.1655C>G
MANE Select
|
NP_001357188.2:p.Thr552Ser
|
|
|
NM_001370260.1:c.1655C>G
|
NP_001357189.1:p.Thr552Ser
|
|
|
NM_001370261.1:c.1655C>G
|
NP_001357190.1:p.Thr552Ser
|
|
|
NM_001370262.1:c.1550C>G
|
NP_001357191.1:p.Thr517Ser
|
|
|
NM_001370263.1:c.1550C>G
|
NP_001357192.1:p.Thr517Ser
|
|
|
NM_000244.4:c.1670C>G
|
NP_000235.3:p.Thr557Ser
|
|
|
NM_001370251.2:c.1781C>G
|
NP_001357180.2:p.Thr594Ser
|
|
|
NM_001370260.2:c.1655C>G
|
NP_001357189.2:p.Thr552Ser
|
|
|
NM_001370261.2:c.1655C>G
|
NP_001357190.2:p.Thr552Ser
|
|
|
NM_001370262.2:c.1550C>G
|
NP_001357191.2:p.Thr517Ser
|
|
|
NM_001370263.2:c.1550C>G
|
NP_001357192.2:p.Thr517Ser
|
|
|
NM_130799.3:c.1655C>G
|
NP_570711.2:p.Thr552Ser
|
|
|
NM_130800.3:c.1670C>G
|
NP_570712.2:p.Thr557Ser
|
|
|
NM_130801.3:c.1670C>G
|
NP_570713.2:p.Thr557Ser
|
|
|
NM_130802.3:c.1670C>G
|
NP_570714.2:p.Thr557Ser
|
|
|
NM_130803.3:c.1670C>G
|
NP_570715.2:p.Thr557Ser
|
|
|
NM_130804.3:c.1670C>G
|
NP_570716.2:p.Thr557Ser
|
|
