ENST00000683611.1:n.1208A>T
|
|
|
ENST00000265104.5:c.13875A>T
MANE Select
|
ENSP00000265104.4:p.Ter4625Tyr
|
|
ENST00000681290.1:c.13830A>T
|
ENSP00000505288.1:p.Ter4610Tyr
|
|
ENST00000265104.4:c.13875A>T
|
ENSP00000265104.4:p.Ter4625Tyr
|
|
NM_001369.2:c.13875A>T
|
NP_001360.1:p.Ter4625Tyr
|
|
XM_005248262.2:c.13830A>T
|
XP_005248319.1:p.Ter4610Tyr
|
|
XM_005248262.3:c.13983A>T
|
XP_005248319.2:p.Ter4661Tyr
|
|
XM_017009177.1:c.13563A>T
|
XP_016864666.1:p.Ter4521Tyr
|
|
XM_017009178.1:c.12888A>T
|
XP_016864667.1:p.Ter4296Tyr
|
|
XM_017009179.2:c.12888A>T
|
XP_016864668.1:p.Ter4296Tyr
|
|
XM_017009185.1:c.9072A>T
|
XP_016864674.1:p.Ter3024Tyr
|
|
XM_017009186.1:c.8625A>T
|
XP_016864675.1:p.Ter2875Tyr
|
|
XM_017009188.1:c.7962A>T
|
XP_016864677.1:p.Ter2654Tyr
|
|
XM_024454388.1:c.12888A>T
|
XP_024310156.1:p.Ter4296Tyr
|
|
XM_024454389.1:c.12477A>T
|
XP_024310157.1:p.Ter4159Tyr
|
|
NM_001369.3:c.13875A>T
MANE Select
|
NP_001360.1:p.Ter4625Tyr
|
|