ENST00000338034.9:c.2324T>C
MANE Select
|
ENSP00000337445.4:p.Ile775Thr
|
|
ENST00000338034.8:c.2324T>C
|
ENSP00000337445.4:p.Ile775Thr
|
|
ENST00000395962.6:c.2267T>C
|
ENSP00000379291.1:p.Ile756Thr
|
|
ENST00000426905.7:c.2204T>C
|
ENSP00000405223.3:p.Ile735Thr
|
|
ENST00000465825.5:n.2211T>C
|
|
|
ENST00000480891.5:n.2153T>C
|
|
|
ENST00000484122.5:n.3154T>C
|
|
|
ENST00000487229.6:n.1870T>C
|
|
|
ENST00000584650.5:c.1723T>C
|
|
|
NM_001165962.1:c.2204T>C
|
NP_001159434.1:p.Ile735Thr
|
|
NM_018127.6:c.2324T>C
|
NP_060597.4:p.Ile775Thr
|
|
NM_173717.1:c.2321T>C
|
NP_776065.1:p.Ile774Thr
|
|
XM_024450850.1:c.2483T>C
|
XP_024306618.1:p.Ile828Thr
|
|
XM_024450851.1:c.2405T>C
|
XP_024306619.1:p.Ile802Thr
|
|
XM_024450852.1:c.2402T>C
|
XP_024306620.1:p.Ile801Thr
|
|
XM_024450853.1:c.2399T>C
|
XP_024306621.1:p.Ile800Thr
|
|
XM_024450854.1:c.2363T>C
|
XP_024306622.1:p.Ile788Thr
|
|
XM_024450855.1:c.2282T>C
|
XP_024306623.1:p.Ile761Thr
|
|
XM_024450856.1:c.2201T>C
|
XP_024306624.1:p.Ile734Thr
|
|
XM_024450857.1:c.2201T>C
|
XP_024306625.1:p.Ile734Thr
|
|
XM_024450858.1:c.2120T>C
|
XP_024306626.1:p.Ile707Thr
|
|
XM_024450859.1:c.2117T>C
|
XP_024306627.1:p.Ile706Thr
|
|
XM_024450860.1:c.2042T>C
|
XP_024306628.1:p.Ile681Thr
|
|
XM_024450861.1:c.2042T>C
|
XP_024306629.1:p.Ile681Thr
|
|
XM_024450862.1:c.2039T>C
|
XP_024306630.1:p.Ile680Thr
|
|
NM_018127.7:c.2324T>C
MANE Select
|
NP_060597.4:p.Ile775Thr
|
|
NM_001165962.2:c.2204T>C
|
NP_001159434.1:p.Ile735Thr
|
|
NM_173717.2:c.2321T>C
|
NP_776065.1:p.Ile774Thr
|
|