ENST00000265104.5:c.9568G>A
MANE Select
|
ENSP00000265104.4:p.Gly3190Arg
|
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ENST00000681290.1:c.9523G>A
|
ENSP00000505288.1:p.Gly3175Arg
|
|
ENST00000265104.4:c.9568G>A
|
ENSP00000265104.4:p.Gly3190Arg
|
|
ENST00000504001.3:n.280G>A
|
|
|
NM_001369.2:c.9568G>A
|
NP_001360.1:p.Gly3190Arg
|
|
XM_005248262.2:c.9523G>A
|
XP_005248319.1:p.Gly3175Arg
|
|
XM_005248262.3:c.9676G>A
|
XP_005248319.2:p.Gly3226Arg
|
|
XM_017009177.1:c.9676G>A
|
XP_016864666.1:p.Gly3226Arg
|
|
XM_017009178.1:c.8581G>A
|
XP_016864667.1:p.Gly2861Arg
|
|
XM_017009179.2:c.8581G>A
|
XP_016864668.1:p.Gly2861Arg
|
|
XM_017009180.1:c.9676G>A
|
XP_016864669.1:p.Gly3226Arg
|
|
XM_017009181.1:c.9676G>A
|
XP_016864670.1:p.Gly3226Arg
|
|
XM_017009182.1:c.9676G>A
|
XP_016864671.1:p.Gly3226Arg
|
|
XM_017009183.1:c.9676G>A
|
XP_016864672.1:p.Gly3226Arg
|
|
XM_017009185.1:c.4765G>A
|
XP_016864674.1:p.Gly1589Arg
|
|
XM_017009186.1:c.4318G>A
|
XP_016864675.1:p.Gly1440Arg
|
|
XM_017009188.1:c.3655G>A
|
XP_016864677.1:p.Gly1219Arg
|
|
XM_024454388.1:c.8581G>A
|
XP_024310156.1:p.Gly2861Arg
|
|
XM_024454389.1:c.8170G>A
|
XP_024310157.1:p.Gly2724Arg
|
|
NM_001369.3:c.9568G>A
MANE Select
|
NP_001360.1:p.Gly3190Arg
|
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