ENST00000265104.5:c.10585T>A
MANE Select
|
ENSP00000265104.4:p.Ser3529Thr
|
|
ENST00000681290.1:c.10540T>A
|
ENSP00000505288.1:p.Ser3514Thr
|
|
ENST00000265104.4:c.10585T>A
|
ENSP00000265104.4:p.Ser3529Thr
|
|
NM_001369.2:c.10585T>A
|
NP_001360.1:p.Ser3529Thr
|
|
XM_005248262.2:c.10540T>A
|
XP_005248319.1:p.Ser3514Thr
|
|
XM_005248262.3:c.10693T>A
|
XP_005248319.2:p.Ser3565Thr
|
|
XM_017009177.1:c.10693T>A
|
XP_016864666.1:p.Ser3565Thr
|
|
XM_017009178.1:c.9598T>A
|
XP_016864667.1:p.Ser3200Thr
|
|
XM_017009179.2:c.9598T>A
|
XP_016864668.1:p.Ser3200Thr
|
|
XM_017009180.1:c.10693T>A
|
XP_016864669.1:p.Ser3565Thr
|
|
XM_017009181.1:c.10693T>A
|
XP_016864670.1:p.Ser3565Thr
|
|
XM_017009182.1:c.10693T>A
|
XP_016864671.1:p.Ser3565Thr
|
|
XM_017009185.1:c.5782T>A
|
XP_016864674.1:p.Ser1928Thr
|
|
XM_017009186.1:c.5335T>A
|
XP_016864675.1:p.Ser1779Thr
|
|
XM_017009188.1:c.4672T>A
|
XP_016864677.1:p.Ser1558Thr
|
|
XM_024454388.1:c.9598T>A
|
XP_024310156.1:p.Ser3200Thr
|
|
XM_024454389.1:c.9187T>A
|
XP_024310157.1:p.Ser3063Thr
|
|
NM_001369.3:c.10585T>A
MANE Select
|
NP_001360.1:p.Ser3529Thr
|
|