ENST00000683611.1:n.1060T>G
|
|
|
ENST00000265104.5:c.13727T>G
MANE Select
|
ENSP00000265104.4:p.Leu4576Ter
|
|
ENST00000681290.1:c.13682T>G
|
ENSP00000505288.1:p.Leu4561Ter
|
|
ENST00000265104.4:c.13727T>G
|
ENSP00000265104.4:p.Leu4576Ter
|
|
NM_001369.2:c.13727T>G
|
NP_001360.1:p.Leu4576Ter
|
|
XM_005248262.2:c.13682T>G
|
XP_005248319.1:p.Leu4561Ter
|
|
XM_005248262.3:c.13835T>G
|
XP_005248319.2:p.Leu4612Ter
|
|
XM_017009177.1:c.13415T>G
|
XP_016864666.1:p.Leu4472Ter
|
|
XM_017009178.1:c.12740T>G
|
XP_016864667.1:p.Leu4247Ter
|
|
XM_017009179.2:c.12740T>G
|
XP_016864668.1:p.Leu4247Ter
|
|
XM_017009185.1:c.8924T>G
|
XP_016864674.1:p.Leu2975Ter
|
|
XM_017009186.1:c.8477T>G
|
XP_016864675.1:p.Leu2826Ter
|
|
XM_017009188.1:c.7814T>G
|
XP_016864677.1:p.Leu2605Ter
|
|
XM_024454388.1:c.12740T>G
|
XP_024310156.1:p.Leu4247Ter
|
|
XM_024454389.1:c.12329T>G
|
XP_024310157.1:p.Leu4110Ter
|
|
NM_001369.3:c.13727T>G
MANE Select
|
NP_001360.1:p.Leu4576Ter
|
|