|
ENST00000642322.2:c.1727C>T
|
ENSP00000496052.2:p.Thr576Met
|
|
|
ENST00000399959.7:c.1592C>T
|
ENSP00000382840.3:p.Thr531Met
|
|
|
ENST00000441189.4:c.1496C>T
|
ENSP00000414281.3:p.Thr499Met
|
|
|
ENST00000457138.7:c.1547C>T
|
ENSP00000392494.2:p.Thr516Met
|
|
|
ENST00000611968.2:c.189C>T
|
|
|
|
ENST00000616050.3:c.343C>T
|
|
|
|
ENST00000629496.3:c.1595C>T
|
ENSP00000487224.1:p.Thr532Met
|
|
|
ENST00000642161.1:n.3794C>T
|
|
|
|
ENST00000642322.1:c.1037C>T
|
ENSP00000496052.1:p.Thr346Met
|
|
|
ENST00000642424.1:c.1037C>T
|
ENSP00000496356.1:p.Thr346Met
|
|
|
ENST00000642589.1:n.4917C>T
|
|
|
|
ENST00000642597.1:n.1769C>T
|
|
|
|
ENST00000642687.1:n.1628C>T
|
|
|
|
ENST00000642722.1:n.2428C>T
|
|
|
|
ENST00000642763.1:n.2486C>T
|
|
|
|
ENST00000642793.1:c.*1044C>T
|
ENSP00000493976.1:n.*1044C>T
|
|
|
ENST00000642801.1:n.1244C>T
|
|
|
|
ENST00000643820.1:n.965C>T
|
|
|
|
ENST00000643963.1:c.*877C>T
|
ENSP00000495264.1:n.*877C>T
|
|
|
ENST00000644073.1:c.1553C>T
|
ENSP00000493475.1:p.Thr518Met
|
|
|
ENST00000644074.1:c.1592C>T
|
ENSP00000496663.1:p.Thr531Met
|
|
|
ENST00000644109.1:c.1757C>T
|
ENSP00000494952.1:p.Thr586Met
|
|
|
ENST00000644307.1:n.1765C>T
|
|
|
|
ENST00000644513.1:c.1595C>T
|
ENSP00000493819.1:p.Thr532Met
|
|
|
ENST00000644677.1:c.1478C>T
|
ENSP00000496524.1:p.Thr493Met
|
|
|
ENST00000644876.2:c.1595C>T
MANE Select
|
ENSP00000494040.1:p.Thr532Met
|
|
|
ENST00000644958.1:n.3256C>T
|
|
|
|
ENST00000645080.1:c.*2817C>T
|
ENSP00000494767.1:n.*2817C>T
|
|
|
ENST00000645120.1:n.3090C>T
|
|
|
|
ENST00000645338.1:n.1765C>T
|
|
|
|
ENST00000645380.1:n.3059C>T
|
|
|
|
ENST00000645561.1:n.2771C>T
|
|
|
|
ENST00000645574.1:n.4459C>T
|
|
|
|
ENST00000645589.1:c.*94C>T
|
ENSP00000494588.1:n.*94C>T
|
|
|
ENST00000646107.1:c.1478C>T
|
ENSP00000494518.1:p.Thr493Met
|
|
|
ENST00000646122.1:c.1595C>T
|
ENSP00000496222.1:p.Thr532Met
|
|
|
ENST00000646196.1:n.2564C>T
|
|
|
|
ENST00000646223.1:c.*1588C>T
|
ENSP00000496043.1:n.*1588C>T
|
|
|
ENST00000646319.1:c.1595C>T
|
ENSP00000495377.1:p.Thr532Met
|
|
|
ENST00000646390.1:n.3883C>T
|
|
|
|
ENST00000646627.1:c.1037C>T
|
ENSP00000493795.1:p.Thr346Met
|
|
|
ENST00000646679.1:c.1037C>T
|
ENSP00000494887.1:p.Thr346Met
|
|
|
ENST00000646822.1:n.2657C>T
|
|
|
|
ENST00000646940.1:n.1769C>T
|
|
|
|
ENST00000647286.1:n.1693C>T
|
|
|
|
ENST00000647477.1:n.334C>T
|
|
|
|
ENST00000399959.6:c.1595C>T
|
ENSP00000382840.2:p.Thr532Met
|
|
|
ENST00000441189.3:c.341-1038C>T
|
ENSP00000414281.2:n.341-1038C>T
|
|
|
ENST00000457138.6:c.1547C>T
|
ENSP00000392494.2:p.Thr516Met
|
|
|
ENST00000478993.5:c.1595C>T
|
ENSP00000478443.1:p.Thr532Met
|
|
|
ENST00000611968.1:c.37C>T
|
|
|
|
ENST00000616050.2:c.148C>T
|
|
|
|
ENST00000625837.2:c.1595C>T
|
ENSP00000486306.1:p.Thr532Met
|
|
|
ENST00000626301.2:c.1595C>T
|
ENSP00000486443.1:p.Thr532Met
|
|
|
ENST00000629496.2:c.1595C>T
|
ENSP00000487224.1:p.Thr532Met
|
|
|
ENST00000629785.2:c.1595C>T
|
ENSP00000486516.1:p.Thr532Met
|
|
|
ENST00000630255.2:c.1595C>T
|
ENSP00000486720.1:p.Thr532Met
|
|
|
ENST00000630370.2:c.1595C>T
|
ENSP00000487062.1:p.Thr532Met
|
|
|
ENST00000630858.2:c.1595C>T
|
ENSP00000486514.1:p.Thr532Met
|
|
|
NM_001193416.2:c.1595C>T
|
NP_001180345.1:p.Thr532Met
|
|
|
NM_001193417.2:c.1547C>T
|
NP_001180346.1:p.Thr516Met
|
|
|
NM_001356.4:c.1595C>T
|
NP_001347.3:p.Thr532Met
|
|
|
NR_126093.1:n.2540C>T
|
|
|
|
XM_011543892.1:c.1595C>T
|
XP_011542194.1:p.Thr532Met
|
|
|
NM_001363819.1:c.1037C>T
|
NP_001350748.1:p.Thr346Met
|
|
|
XM_011543892.2:c.1595C>T
|
XP_011542194.1:p.Thr532Met
|
|
|
XM_017029313.1:c.1037C>T
|
XP_016884802.1:p.Thr346Met
|
|
|
NM_001193416.3:c.1595C>T
|
NP_001180345.1:p.Thr532Met
|
|
|
NM_001193417.3:c.1547C>T
|
NP_001180346.1:p.Thr516Met
|
|
|
NM_001356.5:c.1595C>T
MANE Select
|
NP_001347.3:p.Thr532Met
|
|
