ENST00000290866.10:c.3773G=
MANE Select
|
ENSP00000290866.4:p.Gly1258=
|
|
ENST00000290863.10:c.2051G=
|
ENSP00000290863.6:p.Gly684=
|
|
ENST00000290866.9:c.3773G=
|
ENSP00000290866.4:p.Gly1258=
|
|
ENST00000413513.7:c.1928G=
|
ENSP00000392247.3:p.Gly643=
|
|
ENST00000428043.5:c.*195G=
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ENSP00000397593.2:n.*195G=
|
|
ENST00000577647.2:c.1969+233G=
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ENSP00000464149.1:n.1969+233G=
|
|
ENST00000578839.5:c.*1528G=
|
ENSP00000462110.2:n.*1528G=
|
|
ENST00000579314.5:c.*1502G=
|
ENSP00000462599.1:n.*1502G=
|
|
NM_000789.3:c.3773G=
|
NP_000780.1:p.Gly1258=
|
|
NM_001178057.1:c.1928G=
|
NP_001171528.1:p.Gly643=
|
|
NM_152830.2:c.2051G=
|
NP_690043.1:p.Gly684=
|
|
XM_005257110.1:c.3224G=
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XP_005257167.1:p.Gly1075=
|
|
XM_006721737.2:c.2111G=
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XP_006721800.2:p.Gly704=
|
|
XM_006721737.3:c.2111G=
|
XP_006721800.2:p.Gly704=
|
|
NM_000789.4:c.3773G=
MANE Select
|
NP_000780.1:p.Gly1258=
|
|
NM_001178057.2:c.1928G=
|
NP_001171528.1:p.Gly643=
|
|
NM_152830.3:c.2051G=
|
NP_690043.1:p.Gly684=
|
|
NM_001382700.1:c.3206G=
|
NP_001369629.1:p.Gly1069=
|
|
NM_001382701.1:c.2921G=
|
NP_001369630.1:p.Gly974=
|
|
NM_001382702.1:c.1388G=
|
NP_001369631.1:p.Gly463=
|
|
NR_168483.1:n.2151G=
|
|
|