ENST00000225171.7:c.267G>C
MANE Select
|
ENSP00000225171.2:p.Gln89His
|
|
ENST00000225171.6:c.267G>C
|
ENSP00000225171.2:p.Gln89His
|
|
ENST00000339758.7:c.267G>C
|
ENSP00000343575.6:p.Gln89His
|
|
ENST00000480180.1:c.*286G>C
|
ENSP00000474804.1:n.*286G>C
|
|
ENST00000480963.5:c.*187G>C
|
ENSP00000473979.1:n.*187G>C
|
|
ENST00000483798.6:c.357G>C
|
ENSP00000474215.1:p.Gln119His
|
|
NM_021800.2:c.267G>C
|
NP_068572.1:p.Gln89His
|
|
NM_201262.1:c.267G>C
|
NP_957714.1:p.Gln89His
|
|
XM_011539967.1:c.297G>C
|
XP_011538269.1:p.Gln99His
|
|
XM_017016431.1:c.21G>C
|
XP_016871920.1:p.Gln7His
|
|
XM_017016432.2:c.21G>C
|
XP_016871921.1:p.Gln7His
|
|
NM_021800.3:c.267G>C
MANE Select
|
NP_068572.1:p.Gln89His
|
|
NM_201262.2:c.267G>C
|
NP_957714.1:p.Gln89His
|
|