ENST00000683611.1:n.1208A>G
|
|
|
ENST00000265104.5:c.13875A>G
MANE Select
|
ENSP00000265104.4:p.Ter4625=
|
|
ENST00000681290.1:c.13830A>G
|
ENSP00000505288.1:p.Ter4610=
|
|
ENST00000265104.4:c.13875A>G
|
ENSP00000265104.4:p.Ter4625=
|
|
NM_001369.2:c.13875A>G
|
NP_001360.1:p.Ter4625=
|
|
XM_005248262.2:c.13830A>G
|
XP_005248319.1:p.Ter4610=
|
|
XM_005248262.3:c.13983A>G
|
XP_005248319.2:p.Ter4661=
|
|
XM_017009177.1:c.13563A>G
|
XP_016864666.1:p.Ter4521=
|
|
XM_017009178.1:c.12888A>G
|
XP_016864667.1:p.Ter4296=
|
|
XM_017009179.2:c.12888A>G
|
XP_016864668.1:p.Ter4296=
|
|
XM_017009185.1:c.9072A>G
|
XP_016864674.1:p.Ter3024=
|
|
XM_017009186.1:c.8625A>G
|
XP_016864675.1:p.Ter2875=
|
|
XM_017009188.1:c.7962A>G
|
XP_016864677.1:p.Ter2654=
|
|
XM_024454388.1:c.12888A>G
|
XP_024310156.1:p.Ter4296=
|
|
XM_024454389.1:c.12477A>G
|
XP_024310157.1:p.Ter4159=
|
|
NM_001369.3:c.13875A>G
MANE Select
|
NP_001360.1:p.Ter4625=
|
|