ENST00000265104.5:c.11526T>C
MANE Select
|
ENSP00000265104.4:p.Thr3842=
|
|
ENST00000681290.1:c.11481T>C
|
ENSP00000505288.1:p.Thr3827=
|
|
ENST00000265104.4:c.11526T>C
|
ENSP00000265104.4:p.Thr3842=
|
|
NM_001369.2:c.11526T>C
|
NP_001360.1:p.Thr3842=
|
|
XM_005248262.2:c.11481T>C
|
XP_005248319.1:p.Thr3827=
|
|
XM_005248262.3:c.11634T>C
|
XP_005248319.2:p.Thr3878=
|
|
XM_017009177.1:c.11634T>C
|
XP_016864666.1:p.Thr3878=
|
|
XM_017009178.1:c.10539T>C
|
XP_016864667.1:p.Thr3513=
|
|
XM_017009179.2:c.10539T>C
|
XP_016864668.1:p.Thr3513=
|
|
XM_017009180.1:c.11634T>C
|
XP_016864669.1:p.Thr3878=
|
|
XM_017009181.1:c.11634T>C
|
XP_016864670.1:p.Thr3878=
|
|
XM_017009182.1:c.11390T>C
|
XP_016864671.1:p.Leu3797Pro
|
|
XM_017009185.1:c.6723T>C
|
XP_016864674.1:p.Thr2241=
|
|
XM_017009186.1:c.6276T>C
|
XP_016864675.1:p.Thr2092=
|
|
XM_017009188.1:c.5613T>C
|
XP_016864677.1:p.Thr1871=
|
|
XM_024454388.1:c.10539T>C
|
XP_024310156.1:p.Thr3513=
|
|
XM_024454389.1:c.10128T>C
|
XP_024310157.1:p.Thr3376=
|
|
NM_001369.3:c.11526T>C
MANE Select
|
NP_001360.1:p.Thr3842=
|
|