ENST00000262367.10:c.6995G>T
MANE Select
|
ENSP00000262367.5:p.Gly2332Val
|
|
ENST00000262367.9:c.6995G>T
|
ENSP00000262367.5:p.Gly2332Val
|
|
ENST00000382070.7:c.6881G>T
|
ENSP00000371502.3:p.Gly2294Val
|
|
NM_001079846.1:c.6881G>T
|
NP_001073315.1:p.Gly2294Val
|
|
NM_004380.2:c.6995G>T
|
NP_004371.2:p.Gly2332Val
|
|
XM_005255124.3:c.6950G>T
|
XP_005255181.1:p.Gly2317Val
|
|
XM_005255125.3:c.6578G>T
|
XP_005255182.1:p.Gly2193Val
|
|
XM_006720848.2:c.6734G>T
|
XP_006720911.1:p.Gly2245Val
|
|
XM_011522380.1:c.6941G>T
|
XP_011520682.1:p.Gly2314Val
|
|
XM_011522381.1:c.6242G>T
|
XP_011520683.1:p.Gly2081Val
|
|
XM_005255124.4:c.6950G>T
|
XP_005255181.1:p.Gly2317Val
|
|
XM_005255125.4:c.6578G>T
|
XP_005255182.1:p.Gly2193Val
|
|
XM_006720848.3:c.6734G>T
|
XP_006720911.1:p.Gly2245Val
|
|
XM_011522381.2:c.6242G>T
|
XP_011520683.1:p.Gly2081Val
|
|
XM_017022944.1:c.6989G>T
|
XP_016878433.1:p.Gly2330Val
|
|
NM_004380.3:c.6995G>T
MANE Select
|
NP_004371.2:p.Gly2332Val
|
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