|
NM_001330360.2:c.346G>A
MANE Select
|
NP_001317289.1:p.Gly116Arg
|
|
ENST00000379068.8:c.346G>A
MANE Select
|
ENSP00000368358.3:p.Gly116Arg
|
|
NM_001330360.1:c.346G>A
|
NP_001317289.1:p.Gly116Arg
|
|
NM_001378303.1:c.346G>A
|
NP_001365232.1:p.Gly116Arg
|
|
NM_016937.3:c.328G>A
|
NP_058633.2:p.Gly110Arg
|
|
NM_016937.4:c.328G>A
|
NP_058633.2:p.Gly110Arg
|
|
NR_165482.1:n.293G>A
|
|
|
NR_165483.1:n.390G>A
|
|
|
ENST00000379059.7:c.328G>A
|
ENSP00000368349.3:p.Gly110Arg
|
|
ENST00000379068.7:c.346G>A
|
ENSP00000368358.3:p.Gly116Arg
|
|
ENST00000611764.1:c.328G>A
|
ENSP00000478401.1:p.Gly110Arg
|
|
ENST00000672178.1:c.249G>A
|
ENSP00000500742.1:p.Lys83=
|
|
ENST00000677890.1:c.346G>A
|
ENSP00000503099.1:p.Gly116Arg
|
|
ENST00000678847.1:n.435G>A
|
|
|
XM_005274552.2:c.346G>A
|
XP_005274609.1:p.Gly116Arg
|
|
XM_006724499.1:c.-81G>A
|
XP_006724562.1:n.-81G>A
|
|
XM_006724499.2:c.-81G>A
|
XP_006724562.1:n.-81G>A
|
|
XM_011545540.1:c.346G>A
|
XP_011543842.1:p.Gly116Arg
|
|
XM_011545540.3:c.346G>A
|
XP_011543842.1:p.Gly116Arg
|
|
XM_011545541.1:c.346G>A
|
XP_011543843.1:p.Gly116Arg
|
|
XM_011545541.2:c.346G>A
|
XP_011543843.1:p.Gly116Arg
|
|
XM_017029594.2:c.346G>A
|
XP_016885083.1:p.Gly116Arg
|
|
XM_017029595.2:c.346G>A
|
XP_016885084.1:p.Gly116Arg
|
|
XM_017029596.1:c.346G>A
|
XP_016885085.1:p.Gly116Arg
|
|
XM_024452392.1:c.346G>A
|
XP_024308160.1:p.Gly116Arg
|