ENST00000683611.1:n.1198A>T
|
|
|
ENST00000265104.5:c.13865A>T
MANE Select
|
ENSP00000265104.4:p.Asp4622Val
|
|
ENST00000681290.1:c.13820A>T
|
ENSP00000505288.1:p.Asp4607Val
|
|
ENST00000265104.4:c.13865A>T
|
ENSP00000265104.4:p.Asp4622Val
|
|
NM_001369.2:c.13865A>T
|
NP_001360.1:p.Asp4622Val
|
|
XM_005248262.2:c.13820A>T
|
XP_005248319.1:p.Asp4607Val
|
|
XM_005248262.3:c.13973A>T
|
XP_005248319.2:p.Asp4658Val
|
|
XM_017009177.1:c.13553A>T
|
XP_016864666.1:p.Asp4518Val
|
|
XM_017009178.1:c.12878A>T
|
XP_016864667.1:p.Asp4293Val
|
|
XM_017009179.2:c.12878A>T
|
XP_016864668.1:p.Asp4293Val
|
|
XM_017009185.1:c.9062A>T
|
XP_016864674.1:p.Asp3021Val
|
|
XM_017009186.1:c.8615A>T
|
XP_016864675.1:p.Asp2872Val
|
|
XM_017009188.1:c.7952A>T
|
XP_016864677.1:p.Asp2651Val
|
|
XM_024454388.1:c.12878A>T
|
XP_024310156.1:p.Asp4293Val
|
|
XM_024454389.1:c.12467A>T
|
XP_024310157.1:p.Asp4156Val
|
|
NM_001369.3:c.13865A>T
MANE Select
|
NP_001360.1:p.Asp4622Val
|
|