ENST00000706952.1:c.950G>T
|
ENSP00000516672.1:p.Gly317Val
|
|
ENST00000638630.1:c.80G>T
|
ENSP00000492390.1:p.Gly27Val
|
|
ENST00000640694.1:c.791G>T
|
ENSP00000492403.1:p.Gly264Val
|
|
ENST00000642864.1:c.791G>T
MANE Select
|
ENSP00000495726.1:p.Gly264Val
|
|
ENST00000674510.1:c.791G>T
|
ENSP00000502054.1:p.Gly264Val
|
|
ENST00000675719.1:c.761G>T
|
ENSP00000501927.1:p.Gly254Val
|
|
ENST00000375365.2:c.176G>T
|
ENSP00000364514.2:p.Gly59Val
|
|
ENST00000396435.7:c.791G>T
|
ENSP00000379712.3:p.Gly264Val
|
|
NM_001111125.2:c.791G>T
|
NP_001104595.1:p.Gly264Val
|
|
NM_015075.1:c.176G>T
|
NP_055890.1:p.Gly59Val
|
|
XM_006724579.2:c.887G>T
|
XP_006724642.1:p.Gly296Val
|
|
XM_006724580.2:c.176G>T
|
XP_006724643.1:p.Gly59Val
|
|
XM_006724581.2:c.887G>T
|
XP_006724644.1:p.Gly296Val
|
|
XM_006724582.2:c.887G>T
|
XP_006724645.1:p.Gly296Val
|
|
XM_006724583.2:c.887G>T
|
XP_006724646.1:p.Gly296Val
|
|
XM_006724584.2:c.887G>T
|
XP_006724647.1:p.Gly296Val
|
|
XM_011530772.1:c.113G>T
|
XP_011529074.1:p.Gly38Val
|
|
XM_011530773.1:c.80G>T
|
XP_011529075.1:p.Gly27Val
|
|
XM_011530774.1:c.887G>T
|
XP_011529076.1:p.Gly296Val
|
|
XM_011530775.1:c.887G>T
|
XP_011529077.1:p.Gly296Val
|
|
XM_011530776.1:c.887G>T
|
XP_011529078.1:p.Gly296Val
|
|
XM_011530777.1:c.887G>T
|
XP_011529079.1:p.Gly296Val
|
|
XR_938365.1:n.1114G>T
|
|
|
XM_006724579.3:c.887G>T
|
XP_006724642.1:p.Gly296Val
|
|
XM_006724580.3:c.176G>T
|
XP_006724643.1:p.Gly59Val
|
|
XM_006724581.4:c.887G>T
|
XP_006724644.1:p.Gly296Val
|
|
XM_006724582.4:c.887G>T
|
XP_006724645.1:p.Gly296Val
|
|
XM_006724583.4:c.887G>T
|
XP_006724646.1:p.Gly296Val
|
|
XM_006724584.3:c.887G>T
|
XP_006724647.1:p.Gly296Val
|
|
XM_011530773.2:c.80G>T
|
XP_011529075.1:p.Gly27Val
|
|
XM_011530774.3:c.887G>T
|
XP_011529076.1:p.Gly296Val
|
|
XM_011530776.2:c.887G>T
|
XP_011529078.1:p.Gly296Val
|
|
XM_011530777.2:c.887G>T
|
XP_011529079.1:p.Gly296Val
|
|
XM_017029359.2:c.761G>T
|
XP_016884848.1:p.Gly254Val
|
|
XM_017029360.1:c.293G>T
|
XP_016884849.1:p.Gly98Val
|
|
XR_938365.2:n.1108G>T
|
|
|
NM_001111125.3:c.791G>T
MANE Select
|
NP_001104595.1:p.Gly264Val
|
|
NM_015075.2:c.176G>T
|
NP_055890.1:p.Gly59Val
|
|