ENST00000642322.2:c.1350A>C
|
ENSP00000496052.2:p.Gly450=
|
|
ENST00000399959.7:c.1215A>C
|
ENSP00000382840.3:p.Gly405=
|
|
ENST00000441189.4:c.1119A>C
|
ENSP00000414281.3:p.Gly373=
|
|
ENST00000457138.7:c.1170A>C
|
ENSP00000392494.2:p.Gly390=
|
|
ENST00000629496.3:c.1218A>C
|
ENSP00000487224.1:p.Gly406=
|
|
ENST00000642161.1:n.3417A>C
|
|
|
ENST00000642322.1:c.660A>C
|
ENSP00000496052.1:p.Gly220=
|
|
ENST00000642424.1:c.660A>C
|
ENSP00000496356.1:p.Gly220=
|
|
ENST00000642589.1:n.4540A>C
|
|
|
ENST00000642597.1:n.1392A>C
|
|
|
ENST00000642687.1:n.1251A>C
|
|
|
ENST00000642722.1:n.2051A>C
|
|
|
ENST00000642763.1:n.2109A>C
|
|
|
ENST00000642793.1:c.*667A>C
|
ENSP00000493976.1:n.*667A>C
|
|
ENST00000642801.1:n.867A>C
|
|
|
ENST00000643820.1:n.494A>C
|
|
|
ENST00000643963.1:c.*500A>C
|
ENSP00000495264.1:n.*500A>C
|
|
ENST00000644073.1:c.1176A>C
|
ENSP00000493475.1:p.Gly392=
|
|
ENST00000644074.1:c.1215A>C
|
ENSP00000496663.1:p.Gly405=
|
|
ENST00000644109.1:c.1380A>C
|
ENSP00000494952.1:p.Gly460=
|
|
ENST00000644307.1:n.1388A>C
|
|
|
ENST00000644513.1:c.1218A>C
|
ENSP00000493819.1:p.Gly406=
|
|
ENST00000644677.1:c.1101A>C
|
ENSP00000496524.1:p.Gly367=
|
|
ENST00000644876.2:c.1218A>C
MANE Select
|
ENSP00000494040.1:p.Gly406=
|
|
ENST00000644958.1:n.2879A>C
|
|
|
ENST00000645080.1:c.*2440A>C
|
ENSP00000494767.1:n.*2440A>C
|
|
ENST00000645120.1:n.2713A>C
|
|
|
ENST00000645338.1:n.1388A>C
|
|
|
ENST00000645380.1:n.2682A>C
|
|
|
ENST00000645561.1:n.2394A>C
|
|
|
ENST00000645574.1:n.4082A>C
|
|
|
ENST00000645589.1:c.1218A>C
|
ENSP00000494588.1:p.Gly406=
|
|
ENST00000646093.1:n.402A>C
|
|
|
ENST00000646107.1:c.1101A>C
|
ENSP00000494518.1:p.Gly367=
|
|
ENST00000646122.1:c.1218A>C
|
ENSP00000496222.1:p.Gly406=
|
|
ENST00000646196.1:n.2187A>C
|
|
|
ENST00000646223.1:c.*1211A>C
|
ENSP00000496043.1:n.*1211A>C
|
|
ENST00000646319.1:c.1218A>C
|
ENSP00000495377.1:p.Gly406=
|
|
ENST00000646390.1:n.3506A>C
|
|
|
ENST00000646627.1:c.660A>C
|
ENSP00000493795.1:p.Gly220=
|
|
ENST00000646679.1:c.660A>C
|
ENSP00000494887.1:p.Gly220=
|
|
ENST00000646822.1:n.2280A>C
|
|
|
ENST00000646940.1:n.1392A>C
|
|
|
ENST00000647286.1:n.1316A>C
|
|
|
ENST00000399959.6:c.1218A>C
|
ENSP00000382840.2:p.Gly406=
|
|
ENST00000441189.3:c.341-2189A>C
|
ENSP00000414281.2:n.341-2189A>C
|
|
ENST00000457138.6:c.1170A>C
|
ENSP00000392494.2:p.Gly390=
|
|
ENST00000478993.5:c.1218A>C
|
ENSP00000478443.1:p.Gly406=
|
|
ENST00000542215.5:n.1266A>C
|
|
|
ENST00000625837.2:c.1218A>C
|
ENSP00000486306.1:p.Gly406=
|
|
ENST00000626301.2:c.1218A>C
|
ENSP00000486443.1:p.Gly406=
|
|
ENST00000629496.2:c.1218A>C
|
ENSP00000487224.1:p.Gly406=
|
|
ENST00000629785.2:c.1218A>C
|
ENSP00000486516.1:p.Gly406=
|
|
ENST00000630255.2:c.1218A>C
|
ENSP00000486720.1:p.Gly406=
|
|
ENST00000630370.2:c.1218A>C
|
ENSP00000487062.1:p.Gly406=
|
|
ENST00000630858.2:c.1218A>C
|
ENSP00000486514.1:p.Gly406=
|
|
NM_001193416.2:c.1218A>C
|
NP_001180345.1:p.Gly406=
|
|
NM_001193417.2:c.1170A>C
|
NP_001180346.1:p.Gly390=
|
|
NM_001356.4:c.1218A>C
|
NP_001347.3:p.Gly406=
|
|
NR_126093.1:n.2163A>C
|
|
|
XM_011543892.1:c.1218A>C
|
XP_011542194.1:p.Gly406=
|
|
NM_001363819.1:c.660A>C
|
NP_001350748.1:p.Gly220=
|
|
XM_011543892.2:c.1218A>C
|
XP_011542194.1:p.Gly406=
|
|
XM_017029313.1:c.660A>C
|
XP_016884802.1:p.Gly220=
|
|
NM_001193416.3:c.1218A>C
|
NP_001180345.1:p.Gly406=
|
|
NM_001193417.3:c.1170A>C
|
NP_001180346.1:p.Gly390=
|
|
NM_001356.5:c.1218A>C
MANE Select
|
NP_001347.3:p.Gly406=
|
|