ENST00000350026.11:c.3769G>T
|
ENSP00000055163.8:p.Gly1257Ter
|
|
ENST00000414678.8:c.3838G>T
|
ENSP00000412835.3:p.Gly1280Ter
|
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ENST00000637015.2:c.4057G>T
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ENSP00000489729.2:p.Gly1353Ter
|
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ENST00000346085.10:c.3808G>T
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ENSP00000344546.5:p.Gly1270Ter
|
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ENST00000350026.10:c.3520G>T
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ENSP00000055163.7:p.Gly1174Ter
|
|
ENST00000414678.7:c.2086G>T
|
ENSP00000412835.2:p.Gly696Ter
|
|
ENST00000635849.1:c.1249G>T
|
ENSP00000490948.1:p.Gly417Ter
|
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ENST00000635957.1:c.883G>T
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ENSP00000490385.1:p.Gly295Ter
|
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ENST00000636930.2:c.3928G>T
MANE Select
|
ENSP00000490491.2:p.Gly1310Ter
|
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ENST00000636940.1:n.1925G>T
|
|
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ENST00000637015.1:c.1296G>T
|
|
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ENST00000637568.1:c.1210G>T
|
|
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ENST00000637741.1:n.594G>T
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|
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ENST00000637810.1:c.1270G>T
|
ENSP00000489636.1:p.Gly424Ter
|
|
ENST00000637904.1:c.1429G>T
|
ENSP00000490550.1:p.Gly477Ter
|
|
ENST00000647938.1:c.3559G>T
|
ENSP00000498155.1:p.Gly1187Ter
|
|
ENST00000346085.9:c.3559G>T
|
ENSP00000344546.4:p.Gly1187Ter
|
|
ENST00000350026.9:c.3520G>T
|
ENSP00000055163.7:p.Gly1174Ter
|
|
ENST00000414678.6:c.2086G>T
|
ENSP00000412835.2:p.Gly696Ter
|
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NM_017519.2:c.3520G>T
|
NP_059989.2:p.Gly1174Ter
|
|
NM_020732.3:c.3559G>T
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NP_065783.3:p.Gly1187Ter
|
|
XM_005267069.3:c.3679G>T
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XP_005267126.2:p.Gly1227Ter
|
|
XM_011535984.1:c.2758G>T
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XP_011534286.1:p.Gly920Ter
|
|
XM_011535985.1:c.2578G>T
|
XP_011534287.1:p.Gly860Ter
|
|
XM_011535986.1:c.2338G>T
|
XP_011534288.1:p.Gly780Ter
|
|
XM_011535987.1:c.1957G>T
|
XP_011534289.1:p.Gly653Ter
|
|
XM_011535988.1:c.820G>T
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XP_011534290.1:p.Gly274Ter
|
|
NM_001346813.1:c.3679G>T
|
NP_001333742.1:p.Gly1227Ter
|
|
NM_001363725.1:c.1429G>T
|
NP_001350654.1:p.Gly477Ter
|
|
XM_011535984.2:c.3889G>T
|
XP_011534286.2:p.Gly1297Ter
|
|
XM_011535988.3:c.820G>T
|
XP_011534290.1:p.Gly274Ter
|
|
XM_017011103.2:c.3790G>T
|
XP_016866592.1:p.Gly1264Ter
|
|
XM_017011104.1:c.3760G>T
|
XP_016866593.1:p.Gly1254Ter
|
|
XM_017011105.2:c.3730G>T
|
XP_016866594.1:p.Gly1244Ter
|
|
XM_017011106.2:c.3601G>T
|
XP_016866595.1:p.Gly1201Ter
|
|
XM_017011107.2:c.3580G>T
|
XP_016866596.1:p.Gly1194Ter
|
|
XR_002956289.1:n.3972G>T
|
|
|
NM_001363725.2:c.1429G>T
|
NP_001350654.1:p.Gly477Ter
|
|
NM_001371656.1:c.3808G>T
|
NP_001358585.1:p.Gly1270Ter
|
|
NM_001374820.1:c.3808G>T
|
NP_001361749.1:p.Gly1270Ter
|
|
NM_001374828.1:c.3928G>T
MANE Select
|
NP_001361757.1:p.Gly1310Ter
|
|
NM_017519.3:c.3769G>T
|
NP_059989.3:p.Gly1257Ter
|
|