ENST00000557088.6:c.*1112G>T
|
ENSP00000451002.1:n.*1112G>T
|
|
ENST00000557570.2:c.978G>T
|
ENSP00000450787.2:p.Gln326His
|
|
ENST00000706675.1:n.961G>T
|
|
|
ENST00000706676.1:c.1320G>T
|
ENSP00000516492.1:p.Gln440His
|
|
ENST00000706677.1:c.1146G>T
|
ENSP00000516493.1:p.Gln382His
|
|
ENST00000706678.1:n.1066G>T
|
|
|
ENST00000706679.1:c.978G>T
|
ENSP00000516494.1:p.Gln326His
|
|
ENST00000706680.1:c.*989G>T
|
ENSP00000516495.1:n.*989G>T
|
|
ENST00000706681.1:c.*885G>T
|
ENSP00000516496.1:n.*885G>T
|
|
ENST00000342058.9:c.1146G>T
MANE Select
|
ENSP00000345008.4:p.Gln382His
|
|
ENST00000267620.14:c.1269G>T
|
ENSP00000267620.10:p.Gln423His
|
|
ENST00000342058.8:c.1146G>T
|
ENSP00000345008.4:p.Gln382His
|
|
ENST00000554121.2:n.272G>T
|
|
|
ENST00000556154.5:c.1161G>T
|
ENSP00000451982.1:p.Gln387His
|
|
NM_006329.3:c.1146G>T , LRG_364t1:c.1146G>T
|
NP_006320.2:p.Gln382His
|
|
XM_005267267.3:c.1197G>T
|
XP_005267324.1:p.Gln399His
|
|
XM_011536356.1:c.1197G>T
|
XP_011534658.1:p.Gln399His
|
|
XM_011536357.1:c.1146G>T
|
XP_011534659.1:p.Gln382His
|
|
XM_011536358.1:c.978G>T
|
XP_011534660.1:p.Gln326His
|
|
XM_011536357.2:c.1146G>T
|
XP_011534659.1:p.Gln382His
|
|
XM_011536358.2:c.978G>T
|
XP_011534660.1:p.Gln326His
|
|
XM_017020929.2:c.978G>T
|
XP_016876418.1:p.Gln326His
|
|
NM_001384158.1:c.1269G>T
|
NP_001371087.1:p.Gln423His
|
|
NM_001384159.1:c.1197G>T
|
NP_001371088.1:p.Gln399His
|
|
NM_001384160.1:c.1146G>T
|
NP_001371089.1:p.Gln382His
|
|
NM_001384161.1:c.978G>T
|
NP_001371090.1:p.Gln326His
|
|
NM_001384162.1:c.978G>T
|
NP_001371091.1:p.Gln326His
|
|
NM_006329.4:c.1146G>T
MANE Select
|
NP_006320.2:p.Gln382His
|
|