ENST00000262367.10:c.5420G>T
MANE Select
|
ENSP00000262367.5:p.Gly1807Val
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|
ENST00000262367.9:c.5420G>T
|
ENSP00000262367.5:p.Gly1807Val
|
|
ENST00000382070.7:c.5306G>T
|
ENSP00000371502.3:p.Gly1769Val
|
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NM_001079846.1:c.5306G>T
|
NP_001073315.1:p.Gly1769Val
|
|
NM_004380.2:c.5420G>T
|
NP_004371.2:p.Gly1807Val
|
|
XM_005255124.3:c.5375G>T
|
XP_005255181.1:p.Gly1792Val
|
|
XM_005255125.3:c.5003G>T
|
XP_005255182.1:p.Gly1668Val
|
|
XM_006720848.2:c.5159G>T
|
XP_006720911.1:p.Gly1720Val
|
|
XM_011522380.1:c.5366G>T
|
XP_011520682.1:p.Gly1789Val
|
|
XM_011522381.1:c.4667G>T
|
XP_011520683.1:p.Gly1556Val
|
|
XM_005255124.4:c.5375G>T
|
XP_005255181.1:p.Gly1792Val
|
|
XM_005255125.4:c.5003G>T
|
XP_005255182.1:p.Gly1668Val
|
|
XM_006720848.3:c.5159G>T
|
XP_006720911.1:p.Gly1720Val
|
|
XM_011522381.2:c.4667G>T
|
XP_011520683.1:p.Gly1556Val
|
|
XM_017022944.1:c.5414G>T
|
XP_016878433.1:p.Gly1805Val
|
|
NM_004380.3:c.5420G>T
MANE Select
|
NP_004371.2:p.Gly1807Val
|
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