ENST00000350026.11:c.4534G>T
|
ENSP00000055163.8:p.Gly1512Ter
|
|
ENST00000414678.8:c.4603G>T
|
ENSP00000412835.3:p.Gly1535Ter
|
|
ENST00000637015.2:c.4822G>T
|
ENSP00000489729.2:p.Gly1608Ter
|
|
ENST00000346085.10:c.4573G>T
|
ENSP00000344546.5:p.Gly1525Ter
|
|
ENST00000350026.10:c.4285G>T
|
ENSP00000055163.7:p.Gly1429Ter
|
|
ENST00000414678.7:c.2851G>T
|
ENSP00000412835.2:p.Gly951Ter
|
|
ENST00000635849.1:c.2014G>T
|
ENSP00000490948.1:p.Gly672Ter
|
|
ENST00000635957.1:c.1645G>T
|
ENSP00000490385.1:p.Gly549Ter
|
|
ENST00000636227.1:n.3156G>T
|
|
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ENST00000636254.1:n.613G>T
|
|
|
ENST00000636930.2:c.4693G>T
MANE Select
|
ENSP00000490491.2:p.Gly1565Ter
|
|
ENST00000636940.1:n.2690G>T
|
|
|
ENST00000637015.1:c.2061G>T
|
|
|
ENST00000637568.1:c.1975G>T
|
|
|
ENST00000637741.1:n.1359G>T
|
|
|
ENST00000637810.1:c.2035G>T
|
ENSP00000489636.1:p.Gly679Ter
|
|
ENST00000637904.1:c.2194G>T
|
ENSP00000490550.1:p.Gly732Ter
|
|
ENST00000647938.1:c.4324G>T
|
ENSP00000498155.1:p.Gly1442Ter
|
|
ENST00000346085.9:c.4324G>T
|
ENSP00000344546.4:p.Gly1442Ter
|
|
ENST00000350026.9:c.4285G>T
|
ENSP00000055163.7:p.Gly1429Ter
|
|
ENST00000414678.6:c.2851G>T
|
ENSP00000412835.2:p.Gly951Ter
|
|
NM_017519.2:c.4285G>T
|
NP_059989.2:p.Gly1429Ter
|
|
NM_020732.3:c.4324G>T
|
NP_065783.3:p.Gly1442Ter
|
|
XM_005267069.3:c.4444G>T
|
XP_005267126.2:p.Gly1482Ter
|
|
XM_011535984.1:c.3523G>T
|
XP_011534286.1:p.Gly1175Ter
|
|
XM_011535985.1:c.3343G>T
|
XP_011534287.1:p.Gly1115Ter
|
|
XM_011535986.1:c.3103G>T
|
XP_011534288.1:p.Gly1035Ter
|
|
XM_011535987.1:c.2722G>T
|
XP_011534289.1:p.Gly908Ter
|
|
XM_011535988.1:c.1585G>T
|
XP_011534290.1:p.Gly529Ter
|
|
NM_001346813.1:c.4444G>T
|
NP_001333742.1:p.Gly1482Ter
|
|
NM_001363725.1:c.2194G>T
|
NP_001350654.1:p.Gly732Ter
|
|
XM_011535984.2:c.4654G>T
|
XP_011534286.2:p.Gly1552Ter
|
|
XM_011535988.3:c.1585G>T
|
XP_011534290.1:p.Gly529Ter
|
|
XM_017011103.2:c.4555G>T
|
XP_016866592.1:p.Gly1519Ter
|
|
XM_017011104.1:c.4525G>T
|
XP_016866593.1:p.Gly1509Ter
|
|
XM_017011105.2:c.4495G>T
|
XP_016866594.1:p.Gly1499Ter
|
|
XM_017011106.2:c.4366G>T
|
XP_016866595.1:p.Gly1456Ter
|
|
XM_017011107.2:c.4345G>T
|
XP_016866596.1:p.Gly1449Ter
|
|
XR_002956289.1:n.4640G>T
|
|
|
NM_001363725.2:c.2194G>T
|
NP_001350654.1:p.Gly732Ter
|
|
NM_001371656.1:c.4573G>T
|
NP_001358585.1:p.Gly1525Ter
|
|
NM_001374820.1:c.4573G>T
|
NP_001361749.1:p.Gly1525Ter
|
|
NM_001374828.1:c.4693G>T
MANE Select
|
NP_001361757.1:p.Gly1565Ter
|
|
NM_017519.3:c.4534G>T
|
NP_059989.3:p.Gly1512Ter
|
|