ENST00000350026.11:c.3807C>T
|
ENSP00000055163.8:p.Gly1269=
|
|
ENST00000414678.8:c.3876C>T
|
ENSP00000412835.3:p.Gly1292=
|
|
ENST00000637015.2:c.4095C>T
|
ENSP00000489729.2:p.Gly1365=
|
|
ENST00000346085.10:c.3846C>T
|
ENSP00000344546.5:p.Gly1282=
|
|
ENST00000350026.10:c.3558C>T
|
ENSP00000055163.7:p.Gly1186=
|
|
ENST00000414678.7:c.2124C>T
|
ENSP00000412835.2:p.Gly708=
|
|
ENST00000635849.1:c.1287C>T
|
ENSP00000490948.1:p.Gly429=
|
|
ENST00000635957.1:c.921C>T
|
ENSP00000490385.1:p.Gly307=
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|
ENST00000636930.2:c.3966C>T
MANE Select
|
ENSP00000490491.2:p.Gly1322=
|
|
ENST00000636940.1:n.1963C>T
|
|
|
ENST00000637015.1:c.1334C>T
|
|
|
ENST00000637568.1:c.1248C>T
|
|
|
ENST00000637741.1:n.632C>T
|
|
|
ENST00000637810.1:c.1308C>T
|
ENSP00000489636.1:p.Gly436=
|
|
ENST00000637904.1:c.1467C>T
|
ENSP00000490550.1:p.Gly489=
|
|
ENST00000647938.1:c.3597C>T
|
ENSP00000498155.1:p.Gly1199=
|
|
ENST00000346085.9:c.3597C>T
|
ENSP00000344546.4:p.Gly1199=
|
|
ENST00000350026.9:c.3558C>T
|
ENSP00000055163.7:p.Gly1186=
|
|
ENST00000414678.6:c.2124C>T
|
ENSP00000412835.2:p.Gly708=
|
|
NM_017519.2:c.3558C>T
|
NP_059989.2:p.Gly1186=
|
|
NM_020732.3:c.3597C>T
|
NP_065783.3:p.Gly1199=
|
|
XM_005267069.3:c.3717C>T
|
XP_005267126.2:p.Gly1239=
|
|
XM_011535984.1:c.2796C>T
|
XP_011534286.1:p.Gly932=
|
|
XM_011535985.1:c.2616C>T
|
XP_011534287.1:p.Gly872=
|
|
XM_011535986.1:c.2376C>T
|
XP_011534288.1:p.Gly792=
|
|
XM_011535987.1:c.1995C>T
|
XP_011534289.1:p.Gly665=
|
|
XM_011535988.1:c.858C>T
|
XP_011534290.1:p.Gly286=
|
|
NM_001346813.1:c.3717C>T
|
NP_001333742.1:p.Gly1239=
|
|
NM_001363725.1:c.1467C>T
|
NP_001350654.1:p.Gly489=
|
|
XM_011535984.2:c.3927C>T
|
XP_011534286.2:p.Gly1309=
|
|
XM_011535988.3:c.858C>T
|
XP_011534290.1:p.Gly286=
|
|
XM_017011103.2:c.3828C>T
|
XP_016866592.1:p.Gly1276=
|
|
XM_017011104.1:c.3798C>T
|
XP_016866593.1:p.Gly1266=
|
|
XM_017011105.2:c.3768C>T
|
XP_016866594.1:p.Gly1256=
|
|
XM_017011106.2:c.3639C>T
|
XP_016866595.1:p.Gly1213=
|
|
XM_017011107.2:c.3618C>T
|
XP_016866596.1:p.Gly1206=
|
|
XR_002956289.1:n.4010C>T
|
|
|
NM_001363725.2:c.1467C>T
|
NP_001350654.1:p.Gly489=
|
|
NM_001371656.1:c.3846C>T
|
NP_001358585.1:p.Gly1282=
|
|
NM_001374820.1:c.3846C>T
|
NP_001361749.1:p.Gly1282=
|
|
NM_001374828.1:c.3966C>T
MANE Select
|
NP_001361757.1:p.Gly1322=
|
|
NM_017519.3:c.3807C>T
|
NP_059989.3:p.Gly1269=
|
|