ENST00000642322.2:c.1441G>T
|
ENSP00000496052.2:p.Ala481Ser
|
|
ENST00000399959.7:c.1306G>T
|
ENSP00000382840.3:p.Ala436Ser
|
|
ENST00000441189.4:c.1210G>T
|
ENSP00000414281.3:p.Ala404Ser
|
|
ENST00000457138.7:c.1261G>T
|
ENSP00000392494.2:p.Ala421Ser
|
|
ENST00000616050.3:c.57G>T
|
|
|
ENST00000629496.3:c.1309G>T
|
ENSP00000487224.1:p.Ala437Ser
|
|
ENST00000642161.1:n.3508G>T
|
|
|
ENST00000642322.1:c.751G>T
|
ENSP00000496052.1:p.Ala251Ser
|
|
ENST00000642424.1:c.751G>T
|
ENSP00000496356.1:p.Ala251Ser
|
|
ENST00000642589.1:n.4631G>T
|
|
|
ENST00000642597.1:n.1483G>T
|
|
|
ENST00000642687.1:n.1342G>T
|
|
|
ENST00000642722.1:n.2142G>T
|
|
|
ENST00000642763.1:n.2200G>T
|
|
|
ENST00000642793.1:c.*758G>T
|
ENSP00000493976.1:n.*758G>T
|
|
ENST00000642801.1:n.958G>T
|
|
|
ENST00000643820.1:n.585G>T
|
|
|
ENST00000643963.1:c.*591G>T
|
ENSP00000495264.1:n.*591G>T
|
|
ENST00000644073.1:c.1267G>T
|
ENSP00000493475.1:p.Ala423Ser
|
|
ENST00000644074.1:c.1306G>T
|
ENSP00000496663.1:p.Ala436Ser
|
|
ENST00000644109.1:c.1471G>T
|
ENSP00000494952.1:p.Ala491Ser
|
|
ENST00000644307.1:n.1479G>T
|
|
|
ENST00000644513.1:c.1309G>T
|
ENSP00000493819.1:p.Ala437Ser
|
|
ENST00000644677.1:c.1192G>T
|
ENSP00000496524.1:p.Ala398Ser
|
|
ENST00000644876.2:c.1309G>T
MANE Select
|
ENSP00000494040.1:p.Ala437Ser
|
|
ENST00000644958.1:n.2970G>T
|
|
|
ENST00000645080.1:c.*2531G>T
|
ENSP00000494767.1:n.*2531G>T
|
|
ENST00000645120.1:n.2804G>T
|
|
|
ENST00000645338.1:n.1479G>T
|
|
|
ENST00000645380.1:n.2773G>T
|
|
|
ENST00000645561.1:n.2485G>T
|
|
|
ENST00000645574.1:n.4173G>T
|
|
|
ENST00000645589.1:c.1309G>T
|
ENSP00000494588.1:p.Ala437Ser
|
|
ENST00000646093.1:n.493G>T
|
|
|
ENST00000646107.1:c.1192G>T
|
ENSP00000494518.1:p.Ala398Ser
|
|
ENST00000646122.1:c.1309G>T
|
ENSP00000496222.1:p.Ala437Ser
|
|
ENST00000646196.1:n.2278G>T
|
|
|
ENST00000646223.1:c.*1302G>T
|
ENSP00000496043.1:n.*1302G>T
|
|
ENST00000646319.1:c.1309G>T
|
ENSP00000495377.1:p.Ala437Ser
|
|
ENST00000646390.1:n.3597G>T
|
|
|
ENST00000646627.1:c.751G>T
|
ENSP00000493795.1:p.Ala251Ser
|
|
ENST00000646679.1:c.751G>T
|
ENSP00000494887.1:p.Ala251Ser
|
|
ENST00000646822.1:n.2371G>T
|
|
|
ENST00000646940.1:n.1483G>T
|
|
|
ENST00000647286.1:n.1407G>T
|
|
|
ENST00000647477.1:n.48G>T
|
|
|
ENST00000399959.6:c.1309G>T
|
ENSP00000382840.2:p.Ala437Ser
|
|
ENST00000441189.3:c.341-2098G>T
|
ENSP00000414281.2:n.341-2098G>T
|
|
ENST00000457138.6:c.1261G>T
|
ENSP00000392494.2:p.Ala421Ser
|
|
ENST00000478993.5:c.1309G>T
|
ENSP00000478443.1:p.Ala437Ser
|
|
ENST00000542215.5:n.1357G>T
|
|
|
ENST00000625837.2:c.1309G>T
|
ENSP00000486306.1:p.Ala437Ser
|
|
ENST00000626301.2:c.1309G>T
|
ENSP00000486443.1:p.Ala437Ser
|
|
ENST00000629496.2:c.1309G>T
|
ENSP00000487224.1:p.Ala437Ser
|
|
ENST00000629785.2:c.1309G>T
|
ENSP00000486516.1:p.Ala437Ser
|
|
ENST00000630255.2:c.1309G>T
|
ENSP00000486720.1:p.Ala437Ser
|
|
ENST00000630370.2:c.1309G>T
|
ENSP00000487062.1:p.Ala437Ser
|
|
ENST00000630858.2:c.1309G>T
|
ENSP00000486514.1:p.Ala437Ser
|
|
NM_001193416.2:c.1309G>T
|
NP_001180345.1:p.Ala437Ser
|
|
NM_001193417.2:c.1261G>T
|
NP_001180346.1:p.Ala421Ser
|
|
NM_001356.4:c.1309G>T
|
NP_001347.3:p.Ala437Ser
|
|
NR_126093.1:n.2254G>T
|
|
|
XM_011543892.1:c.1309G>T
|
XP_011542194.1:p.Ala437Ser
|
|
NM_001363819.1:c.751G>T
|
NP_001350748.1:p.Ala251Ser
|
|
XM_011543892.2:c.1309G>T
|
XP_011542194.1:p.Ala437Ser
|
|
XM_017029313.1:c.751G>T
|
XP_016884802.1:p.Ala251Ser
|
|
NM_001193416.3:c.1309G>T
|
NP_001180345.1:p.Ala437Ser
|
|
NM_001193417.3:c.1261G>T
|
NP_001180346.1:p.Ala421Ser
|
|
NM_001356.5:c.1309G>T
MANE Select
|
NP_001347.3:p.Ala437Ser
|
|