ENST00000265104.5:c.9292A>G
MANE Select
|
ENSP00000265104.4:p.Arg3098Gly
|
|
ENST00000681290.1:c.9247A>G
|
ENSP00000505288.1:p.Arg3083Gly
|
|
ENST00000265104.4:c.9292A>G
|
ENSP00000265104.4:p.Arg3098Gly
|
|
NM_001369.2:c.9292A>G
|
NP_001360.1:p.Arg3098Gly
|
|
XM_005248262.2:c.9247A>G
|
XP_005248319.1:p.Arg3083Gly
|
|
XM_005248262.3:c.9400A>G
|
XP_005248319.2:p.Arg3134Gly
|
|
XM_017009177.1:c.9400A>G
|
XP_016864666.1:p.Arg3134Gly
|
|
XM_017009178.1:c.8305A>G
|
XP_016864667.1:p.Arg2769Gly
|
|
XM_017009179.2:c.8305A>G
|
XP_016864668.1:p.Arg2769Gly
|
|
XM_017009180.1:c.9400A>G
|
XP_016864669.1:p.Arg3134Gly
|
|
XM_017009181.1:c.9400A>G
|
XP_016864670.1:p.Arg3134Gly
|
|
XM_017009182.1:c.9400A>G
|
XP_016864671.1:p.Arg3134Gly
|
|
XM_017009183.1:c.9400A>G
|
XP_016864672.1:p.Arg3134Gly
|
|
XM_017009185.1:c.4489A>G
|
XP_016864674.1:p.Arg1497Gly
|
|
XM_017009186.1:c.4042A>G
|
XP_016864675.1:p.Arg1348Gly
|
|
XM_017009188.1:c.3379A>G
|
XP_016864677.1:p.Arg1127Gly
|
|
XM_024454388.1:c.8305A>G
|
XP_024310156.1:p.Arg2769Gly
|
|
XM_024454389.1:c.7894A>G
|
XP_024310157.1:p.Arg2632Gly
|
|
NM_001369.3:c.9292A>G
MANE Select
|
NP_001360.1:p.Arg3098Gly
|
|