ENST00000350026.11:c.3543G>C
|
ENSP00000055163.8:p.Gly1181=
|
|
ENST00000414678.8:c.3612G>C
|
ENSP00000412835.3:p.Gly1204=
|
|
ENST00000637015.2:c.3831G>C
|
ENSP00000489729.2:p.Gly1277=
|
|
ENST00000319584.11:c.1716G>C
|
ENSP00000313006.7:p.Gly572=
|
|
ENST00000346085.10:c.3582G>C
|
ENSP00000344546.5:p.Gly1194=
|
|
ENST00000350026.10:c.3294G>C
|
ENSP00000055163.7:p.Gly1098=
|
|
ENST00000414678.7:c.1860G>C
|
ENSP00000412835.2:p.Gly620=
|
|
ENST00000635849.1:c.1023G>C
|
ENSP00000490948.1:p.Gly341=
|
|
ENST00000635957.1:c.657G>C
|
ENSP00000490385.1:p.Gly219=
|
|
ENST00000636930.2:c.3702G>C
MANE Select
|
ENSP00000490491.2:p.Gly1234=
|
|
ENST00000636940.1:n.1699G>C
|
|
|
ENST00000637015.1:c.1070G>C
|
|
|
ENST00000637568.1:c.984G>C
|
|
|
ENST00000637741.1:n.368G>C
|
|
|
ENST00000637810.1:c.1044G>C
|
ENSP00000489636.1:p.Gly348=
|
|
ENST00000637904.1:c.1203G>C
|
ENSP00000490550.1:p.Gly401=
|
|
ENST00000647938.1:c.3333G>C
|
ENSP00000498155.1:p.Gly1111=
|
|
ENST00000319584.10:c.1719G>C
|
ENSP00000313006.6:p.Gly573=
|
|
ENST00000346085.9:c.3333G>C
|
ENSP00000344546.4:p.Gly1111=
|
|
ENST00000350026.9:c.3294G>C
|
ENSP00000055163.7:p.Gly1098=
|
|
ENST00000400790.3:c.495G>C
|
ENSP00000383596.3:p.Gly165=
|
|
ENST00000414678.6:c.1860G>C
|
ENSP00000412835.2:p.Gly620=
|
|
ENST00000478761.3:c.904G>C
|
|
|
NM_017519.2:c.3294G>C
|
NP_059989.2:p.Gly1098=
|
|
NM_020732.3:c.3333G>C
|
NP_065783.3:p.Gly1111=
|
|
XM_005267069.3:c.3453G>C
|
XP_005267126.2:p.Gly1151=
|
|
XM_011535984.1:c.2532G>C
|
XP_011534286.1:p.Gly844=
|
|
XM_011535985.1:c.2352G>C
|
XP_011534287.1:p.Gly784=
|
|
XM_011535986.1:c.2112G>C
|
XP_011534288.1:p.Gly704=
|
|
XM_011535987.1:c.1731G>C
|
XP_011534289.1:p.Gly577=
|
|
XM_011535988.1:c.594G>C
|
XP_011534290.1:p.Gly198=
|
|
NM_001346813.1:c.3453G>C
|
NP_001333742.1:p.Gly1151=
|
|
NM_001363725.1:c.1203G>C
|
NP_001350654.1:p.Gly401=
|
|
XM_011535984.2:c.3663G>C
|
XP_011534286.2:p.Gly1221=
|
|
XM_011535988.3:c.594G>C
|
XP_011534290.1:p.Gly198=
|
|
XM_017011103.2:c.3564G>C
|
XP_016866592.1:p.Gly1188=
|
|
XM_017011104.1:c.3534G>C
|
XP_016866593.1:p.Gly1178=
|
|
XM_017011105.2:c.3504G>C
|
XP_016866594.1:p.Gly1168=
|
|
XM_017011106.2:c.3375G>C
|
XP_016866595.1:p.Gly1125=
|
|
XM_017011107.2:c.3354G>C
|
XP_016866596.1:p.Gly1118=
|
|
XR_002956289.1:n.3746G>C
|
|
|
NM_001363725.2:c.1203G>C
|
NP_001350654.1:p.Gly401=
|
|
NM_001371656.1:c.3582G>C
|
NP_001358585.1:p.Gly1194=
|
|
NM_001374820.1:c.3582G>C
|
NP_001361749.1:p.Gly1194=
|
|
NM_001374828.1:c.3702G>C
MANE Select
|
NP_001361757.1:p.Gly1234=
|
|
NM_017519.3:c.3543G>C
|
NP_059989.3:p.Gly1181=
|
|