ENST00000683611.1:n.809A>T
|
|
|
ENST00000265104.5:c.13476A>T
MANE Select
|
ENSP00000265104.4:p.Leu4492Phe
|
|
ENST00000681290.1:c.13431A>T
|
ENSP00000505288.1:p.Leu4477Phe
|
|
ENST00000265104.4:c.13476A>T
|
ENSP00000265104.4:p.Leu4492Phe
|
|
NM_001369.2:c.13476A>T
|
NP_001360.1:p.Leu4492Phe
|
|
XM_005248262.2:c.13431A>T
|
XP_005248319.1:p.Leu4477Phe
|
|
XM_005248262.3:c.13584A>T
|
XP_005248319.2:p.Leu4528Phe
|
|
XM_017009177.1:c.13164A>T
|
XP_016864666.1:p.Leu4388Phe
|
|
XM_017009178.1:c.12489A>T
|
XP_016864667.1:p.Leu4163Phe
|
|
XM_017009179.2:c.12489A>T
|
XP_016864668.1:p.Leu4163Phe
|
|
XM_017009185.1:c.8673A>T
|
XP_016864674.1:p.Leu2891Phe
|
|
XM_017009186.1:c.8226A>T
|
XP_016864675.1:p.Leu2742Phe
|
|
XM_017009188.1:c.7563A>T
|
XP_016864677.1:p.Leu2521Phe
|
|
XM_024454388.1:c.12489A>T
|
XP_024310156.1:p.Leu4163Phe
|
|
XM_024454389.1:c.12078A>T
|
XP_024310157.1:p.Leu4026Phe
|
|
NM_001369.3:c.13476A>T
MANE Select
|
NP_001360.1:p.Leu4492Phe
|
|