ENST00000262367.10:c.5420G>C
MANE Select
|
ENSP00000262367.5:p.Gly1807Ala
|
|
ENST00000262367.9:c.5420G>C
|
ENSP00000262367.5:p.Gly1807Ala
|
|
ENST00000382070.7:c.5306G>C
|
ENSP00000371502.3:p.Gly1769Ala
|
|
NM_001079846.1:c.5306G>C
|
NP_001073315.1:p.Gly1769Ala
|
|
NM_004380.2:c.5420G>C
|
NP_004371.2:p.Gly1807Ala
|
|
XM_005255124.3:c.5375G>C
|
XP_005255181.1:p.Gly1792Ala
|
|
XM_005255125.3:c.5003G>C
|
XP_005255182.1:p.Gly1668Ala
|
|
XM_006720848.2:c.5159G>C
|
XP_006720911.1:p.Gly1720Ala
|
|
XM_011522380.1:c.5366G>C
|
XP_011520682.1:p.Gly1789Ala
|
|
XM_011522381.1:c.4667G>C
|
XP_011520683.1:p.Gly1556Ala
|
|
XM_005255124.4:c.5375G>C
|
XP_005255181.1:p.Gly1792Ala
|
|
XM_005255125.4:c.5003G>C
|
XP_005255182.1:p.Gly1668Ala
|
|
XM_006720848.3:c.5159G>C
|
XP_006720911.1:p.Gly1720Ala
|
|
XM_011522381.2:c.4667G>C
|
XP_011520683.1:p.Gly1556Ala
|
|
XM_017022944.1:c.5414G>C
|
XP_016878433.1:p.Gly1805Ala
|
|
NM_004380.3:c.5420G>C
MANE Select
|
NP_004371.2:p.Gly1807Ala
|
|