ENST00000350026.11:c.4992G>A
|
ENSP00000055163.8:p.Gly1664=
|
|
ENST00000414678.8:c.5061G>A
|
ENSP00000412835.3:p.Gly1687=
|
|
ENST00000637015.2:c.5280G>A
|
ENSP00000489729.2:p.Gly1760=
|
|
ENST00000346085.10:c.5031G>A
|
ENSP00000344546.5:p.Gly1677=
|
|
ENST00000350026.10:c.4743G>A
|
ENSP00000055163.7:p.Gly1581=
|
|
ENST00000414678.7:c.3309G>A
|
ENSP00000412835.2:p.Gly1103=
|
|
ENST00000635849.1:c.2472G>A
|
ENSP00000490948.1:p.Gly824=
|
|
ENST00000635957.1:c.2103G>A
|
ENSP00000490385.1:p.Gly701=
|
|
ENST00000636227.1:n.3614G>A
|
|
|
ENST00000636254.1:n.1071G>A
|
|
|
ENST00000636930.2:c.5151G>A
MANE Select
|
ENSP00000490491.2:p.Gly1717=
|
|
ENST00000636940.1:n.3148G>A
|
|
|
ENST00000637015.1:c.2519G>A
|
|
|
ENST00000637568.1:c.2433G>A
|
|
|
ENST00000637741.1:n.1817G>A
|
|
|
ENST00000637810.1:c.2493G>A
|
ENSP00000489636.1:p.Gly831=
|
|
ENST00000637904.1:c.2652G>A
|
ENSP00000490550.1:p.Gly884=
|
|
ENST00000647938.1:c.4782G>A
|
ENSP00000498155.1:p.Gly1594=
|
|
ENST00000346085.9:c.4782G>A
|
ENSP00000344546.4:p.Gly1594=
|
|
ENST00000350026.9:c.4743G>A
|
ENSP00000055163.7:p.Gly1581=
|
|
ENST00000414678.6:c.3309G>A
|
ENSP00000412835.2:p.Gly1103=
|
|
NM_017519.2:c.4743G>A
|
NP_059989.2:p.Gly1581=
|
|
NM_020732.3:c.4782G>A
|
NP_065783.3:p.Gly1594=
|
|
XM_005267069.3:c.4902G>A
|
XP_005267126.2:p.Gly1634=
|
|
XM_011535984.1:c.3981G>A
|
XP_011534286.1:p.Gly1327=
|
|
XM_011535985.1:c.3801G>A
|
XP_011534287.1:p.Gly1267=
|
|
XM_011535986.1:c.3561G>A
|
XP_011534288.1:p.Gly1187=
|
|
XM_011535987.1:c.3180G>A
|
XP_011534289.1:p.Gly1060=
|
|
XM_011535988.1:c.2043G>A
|
XP_011534290.1:p.Gly681=
|
|
NM_001346813.1:c.4902G>A
|
NP_001333742.1:p.Gly1634=
|
|
NM_001363725.1:c.2652G>A
|
NP_001350654.1:p.Gly884=
|
|
XM_011535984.2:c.5112G>A
|
XP_011534286.2:p.Gly1704=
|
|
XM_011535988.3:c.2043G>A
|
XP_011534290.1:p.Gly681=
|
|
XM_017011103.2:c.5013G>A
|
XP_016866592.1:p.Gly1671=
|
|
XM_017011104.1:c.4983G>A
|
XP_016866593.1:p.Gly1661=
|
|
XM_017011105.2:c.4953G>A
|
XP_016866594.1:p.Gly1651=
|
|
XM_017011106.2:c.4824G>A
|
XP_016866595.1:p.Gly1608=
|
|
XM_017011107.2:c.4803G>A
|
XP_016866596.1:p.Gly1601=
|
|
XR_002956289.1:n.5098G>A
|
|
|
NM_001363725.2:c.2652G>A
|
NP_001350654.1:p.Gly884=
|
|
NM_001371656.1:c.5031G>A
|
NP_001358585.1:p.Gly1677=
|
|
NM_001374820.1:c.5031G>A
|
NP_001361749.1:p.Gly1677=
|
|
NM_001374828.1:c.5151G>A
MANE Select
|
NP_001361757.1:p.Gly1717=
|
|
NM_017519.3:c.4992G>A
|
NP_059989.3:p.Gly1664=
|
|