ENST00000265104.5:c.10879T>A
MANE Select
|
ENSP00000265104.4:p.Ser3627Thr
|
|
ENST00000681290.1:c.10834T>A
|
ENSP00000505288.1:p.Ser3612Thr
|
|
ENST00000265104.4:c.10879T>A
|
ENSP00000265104.4:p.Ser3627Thr
|
|
NM_001369.2:c.10879T>A
|
NP_001360.1:p.Ser3627Thr
|
|
XM_005248262.2:c.10834T>A
|
XP_005248319.1:p.Ser3612Thr
|
|
XM_005248262.3:c.10987T>A
|
XP_005248319.2:p.Ser3663Thr
|
|
XM_017009177.1:c.10987T>A
|
XP_016864666.1:p.Ser3663Thr
|
|
XM_017009178.1:c.9892T>A
|
XP_016864667.1:p.Ser3298Thr
|
|
XM_017009179.2:c.9892T>A
|
XP_016864668.1:p.Ser3298Thr
|
|
XM_017009180.1:c.10987T>A
|
XP_016864669.1:p.Ser3663Thr
|
|
XM_017009181.1:c.10987T>A
|
XP_016864670.1:p.Ser3663Thr
|
|
XM_017009182.1:c.10987T>A
|
XP_016864671.1:p.Ser3663Thr
|
|
XM_017009185.1:c.6076T>A
|
XP_016864674.1:p.Ser2026Thr
|
|
XM_017009186.1:c.5629T>A
|
XP_016864675.1:p.Ser1877Thr
|
|
XM_017009188.1:c.4966T>A
|
XP_016864677.1:p.Ser1656Thr
|
|
XM_024454388.1:c.9892T>A
|
XP_024310156.1:p.Ser3298Thr
|
|
XM_024454389.1:c.9481T>A
|
XP_024310157.1:p.Ser3161Thr
|
|
NM_001369.3:c.10879T>A
MANE Select
|
NP_001360.1:p.Ser3627Thr
|
|