ENST00000355808.10:c.626G>T
|
ENSP00000348062.6:p.Gly209Val
|
|
ENST00000379805.4:c.*297G>T
|
ENSP00000369133.3:n.*297G>T
|
|
ENST00000417819.6:c.689G>T
|
ENSP00000404616.2:p.Gly230Val
|
|
ENST00000423505.6:c.719G>T
|
ENSP00000406473.2:p.Gly240Val
|
|
ENST00000481733.2:n.400G>T
|
|
|
ENST00000696704.1:c.420G>T
|
ENSP00000512823.1:p.Gly140=
|
|
ENST00000696705.1:c.*60G>T
|
ENSP00000512824.1:n.*60G>T
|
|
ENST00000422285.7:c.605G>T
MANE Select
|
ENSP00000394382.2:p.Gly202Val
|
|
ENST00000379806.9:c.719G>T
|
ENSP00000369134.5:p.Gly240Val
|
|
ENST00000422285.6:c.605G>T
|
ENSP00000394382.2:p.Gly202Val
|
|
ENST00000479146.1:n.440G>T
|
|
|
ENST00000481733.1:n.33G>T
|
|
|
ENST00000540249.5:c.512G>T
|
ENSP00000440761.1:p.Gly171Val
|
|
ENST00000545074.5:c.626G>T
|
ENSP00000438550.1:p.Gly209Val
|
|
NM_000284.3:c.605G>T
|
NP_000275.1:p.Gly202Val
|
|
NM_001173454.1:c.719G>T
|
NP_001166925.1:p.Gly240Val
|
|
NM_001173455.1:c.626G>T
|
NP_001166926.1:p.Gly209Val
|
|
NM_001173456.1:c.512G>T
|
NP_001166927.1:p.Gly171Val
|
|
XM_011545531.1:c.740G>T
|
XP_011543833.1:p.Gly247Val
|
|
XM_011545532.1:c.647G>T
|
XP_011543834.1:p.Gly216Val
|
|
XM_017029574.2:c.626G>T
|
XP_016885063.1:p.Gly209Val
|
|
NM_000284.4:c.605G>T
MANE Select
|
NP_000275.1:p.Gly202Val
|
|
NM_001173454.2:c.719G>T
|
NP_001166925.1:p.Gly240Val
|
|
NM_001173455.2:c.626G>T
|
NP_001166926.1:p.Gly209Val
|
|
NM_001173456.2:c.512G>T
|
NP_001166927.1:p.Gly171Val
|
|