ENST00000683611.1:n.808T>G
|
|
|
ENST00000265104.5:c.13475T>G
MANE Select
|
ENSP00000265104.4:p.Leu4492Ter
|
|
ENST00000681290.1:c.13430T>G
|
ENSP00000505288.1:p.Leu4477Ter
|
|
ENST00000265104.4:c.13475T>G
|
ENSP00000265104.4:p.Leu4492Ter
|
|
NM_001369.2:c.13475T>G
|
NP_001360.1:p.Leu4492Ter
|
|
XM_005248262.2:c.13430T>G
|
XP_005248319.1:p.Leu4477Ter
|
|
XM_005248262.3:c.13583T>G
|
XP_005248319.2:p.Leu4528Ter
|
|
XM_017009177.1:c.13163T>G
|
XP_016864666.1:p.Leu4388Ter
|
|
XM_017009178.1:c.12488T>G
|
XP_016864667.1:p.Leu4163Ter
|
|
XM_017009179.2:c.12488T>G
|
XP_016864668.1:p.Leu4163Ter
|
|
XM_017009185.1:c.8672T>G
|
XP_016864674.1:p.Leu2891Ter
|
|
XM_017009186.1:c.8225T>G
|
XP_016864675.1:p.Leu2742Ter
|
|
XM_017009188.1:c.7562T>G
|
XP_016864677.1:p.Leu2521Ter
|
|
XM_024454388.1:c.12488T>G
|
XP_024310156.1:p.Leu4163Ter
|
|
XM_024454389.1:c.12077T>G
|
XP_024310157.1:p.Leu4026Ter
|
|
NM_001369.3:c.13475T>G
MANE Select
|
NP_001360.1:p.Leu4492Ter
|
|