ENST00000350026.11:c.2763T>A
|
ENSP00000055163.8:p.Gly921=
|
|
ENST00000414678.8:c.2673T>A
|
ENSP00000412835.3:p.Gly891=
|
|
ENST00000637015.2:c.2763T>A
|
ENSP00000489729.2:p.Gly921=
|
|
ENST00000319584.11:c.777T>A
|
ENSP00000313006.7:p.Gly259=
|
|
ENST00000346085.10:c.2802T>A
|
ENSP00000344546.5:p.Gly934=
|
|
ENST00000350026.10:c.2514T>A
|
ENSP00000055163.7:p.Gly838=
|
|
ENST00000414678.7:c.921T>A
|
ENSP00000412835.2:p.Gly307=
|
|
ENST00000452544.2:n.664T>A
|
|
|
ENST00000635849.1:c.84T>A
|
ENSP00000490948.1:p.Gly28=
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|
ENST00000636930.2:c.2763T>A
MANE Select
|
ENSP00000490491.2:p.Gly921=
|
|
ENST00000637015.1:c.2T>A
|
|
|
ENST00000637810.1:c.264T>A
|
ENSP00000489636.1:p.Gly88=
|
|
ENST00000637904.1:c.264T>A
|
ENSP00000490550.1:p.Gly88=
|
|
ENST00000647938.1:c.2553T>A
|
ENSP00000498155.1:p.Gly851=
|
|
ENST00000674190.1:n.1512T>A
|
|
|
ENST00000319584.10:c.780T>A
|
ENSP00000313006.6:p.Gly260=
|
|
ENST00000346085.9:c.2553T>A
|
ENSP00000344546.4:p.Gly851=
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|
ENST00000350026.9:c.2514T>A
|
ENSP00000055163.7:p.Gly838=
|
|
ENST00000414678.6:c.921T>A
|
ENSP00000412835.2:p.Gly307=
|
|
ENST00000452544.1:n.610T>A
|
|
|
NM_017519.2:c.2514T>A
|
NP_059989.2:p.Gly838=
|
|
NM_020732.3:c.2553T>A
|
NP_065783.3:p.Gly851=
|
|
XM_005267069.3:c.2514T>A
|
XP_005267126.2:p.Gly838=
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|
XM_011535984.1:c.1464T>A
|
XP_011534286.1:p.Gly488=
|
|
XM_011535985.1:c.1284T>A
|
XP_011534287.1:p.Gly428=
|
|
XM_011535986.1:c.1044T>A
|
XP_011534288.1:p.Gly348=
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|
XM_011535987.1:c.663T>A
|
XP_011534289.1:p.Gly221=
|
|
XM_011535988.1:c.-20+15418T>A
|
XP_011534290.1:n.-20+15418T>A
|
|
NM_001346813.1:c.2514T>A
|
NP_001333742.1:p.Gly838=
|
|
NM_001363725.1:c.264T>A
|
NP_001350654.1:p.Gly88=
|
|
XM_011535984.2:c.2595T>A
|
XP_011534286.2:p.Gly865=
|
|
XM_011535988.3:c.-20+15418T>A
|
XP_011534290.1:n.-20+15418T>A
|
|
XM_017011103.2:c.2595T>A
|
XP_016866592.1:p.Gly865=
|
|
XM_017011104.1:c.2595T>A
|
XP_016866593.1:p.Gly865=
|
|
XM_017011105.2:c.2595T>A
|
XP_016866594.1:p.Gly865=
|
|
XM_017011106.2:c.2595T>A
|
XP_016866595.1:p.Gly865=
|
|
XM_017011107.2:c.2415T>A
|
XP_016866596.1:p.Gly805=
|
|
XR_002956289.1:n.2678T>A
|
|
|
NM_001363725.2:c.264T>A
|
NP_001350654.1:p.Gly88=
|
|
NM_001371656.1:c.2802T>A
|
NP_001358585.1:p.Gly934=
|
|
NM_001374820.1:c.2802T>A
|
NP_001361749.1:p.Gly934=
|
|
NM_001374828.1:c.2763T>A
MANE Select
|
NP_001361757.1:p.Gly921=
|
|
NM_017519.3:c.2763T>A
|
NP_059989.3:p.Gly921=
|
|