ENST00000683611.1:n.559G>T
|
|
|
ENST00000265104.5:c.13226G>T
MANE Select
|
ENSP00000265104.4:p.Ser4409Ile
|
|
ENST00000681290.1:c.13181G>T
|
ENSP00000505288.1:p.Ser4394Ile
|
|
ENST00000265104.4:c.13226G>T
|
ENSP00000265104.4:p.Ser4409Ile
|
|
NM_001369.2:c.13226G>T
|
NP_001360.1:p.Ser4409Ile
|
|
XM_005248262.2:c.13181G>T
|
XP_005248319.1:p.Ser4394Ile
|
|
XM_005248262.3:c.13334G>T
|
XP_005248319.2:p.Ser4445Ile
|
|
XM_017009177.1:c.12914G>T
|
XP_016864666.1:p.Ser4305Ile
|
|
XM_017009178.1:c.12239G>T
|
XP_016864667.1:p.Ser4080Ile
|
|
XM_017009179.2:c.12239G>T
|
XP_016864668.1:p.Ser4080Ile
|
|
XM_017009185.1:c.8423G>T
|
XP_016864674.1:p.Ser2808Ile
|
|
XM_017009186.1:c.7976G>T
|
XP_016864675.1:p.Ser2659Ile
|
|
XM_017009188.1:c.7313G>T
|
XP_016864677.1:p.Ser2438Ile
|
|
XM_024454388.1:c.12239G>T
|
XP_024310156.1:p.Ser4080Ile
|
|
XM_024454389.1:c.11828G>T
|
XP_024310157.1:p.Ser3943Ile
|
|
NM_001369.3:c.13226G>T
MANE Select
|
NP_001360.1:p.Ser4409Ile
|
|