ENST00000265104.5:c.10930G>A
MANE Select
|
ENSP00000265104.4:p.Gly3644Arg
|
|
ENST00000681290.1:c.10885G>A
|
ENSP00000505288.1:p.Gly3629Arg
|
|
ENST00000265104.4:c.10930G>A
|
ENSP00000265104.4:p.Gly3644Arg
|
|
NM_001369.2:c.10930G>A
|
NP_001360.1:p.Gly3644Arg
|
|
XM_005248262.2:c.10885G>A
|
XP_005248319.1:p.Gly3629Arg
|
|
XM_005248262.3:c.11038G>A
|
XP_005248319.2:p.Gly3680Arg
|
|
XM_017009177.1:c.11038G>A
|
XP_016864666.1:p.Gly3680Arg
|
|
XM_017009178.1:c.9943G>A
|
XP_016864667.1:p.Gly3315Arg
|
|
XM_017009179.2:c.9943G>A
|
XP_016864668.1:p.Gly3315Arg
|
|
XM_017009180.1:c.11038G>A
|
XP_016864669.1:p.Gly3680Arg
|
|
XM_017009181.1:c.11038G>A
|
XP_016864670.1:p.Gly3680Arg
|
|
XM_017009182.1:c.11038G>A
|
XP_016864671.1:p.Gly3680Arg
|
|
XM_017009185.1:c.6127G>A
|
XP_016864674.1:p.Gly2043Arg
|
|
XM_017009186.1:c.5680G>A
|
XP_016864675.1:p.Gly1894Arg
|
|
XM_017009188.1:c.5017G>A
|
XP_016864677.1:p.Gly1673Arg
|
|
XM_024454388.1:c.9943G>A
|
XP_024310156.1:p.Gly3315Arg
|
|
XM_024454389.1:c.9532G>A
|
XP_024310157.1:p.Gly3178Arg
|
|
NM_001369.3:c.10930G>A
MANE Select
|
NP_001360.1:p.Gly3644Arg
|
|