ENST00000696217.1:n.499C>T
|
|
|
ENST00000219150.10:c.418C>T
MANE Select
|
ENSP00000219150.6:p.His140Tyr
|
|
ENST00000219150.9:c.418C>T
|
ENSP00000219150.5:p.His140Tyr
|
|
ENST00000561815.5:c.526C>T
|
ENSP00000456756.1:p.His176Tyr
|
|
ENST00000563778.5:c.418C>T
|
ENSP00000456266.1:p.His140Tyr
|
|
ENST00000564768.1:n.231C>T
|
|
|
ENST00000565497.5:c.418C>T
|
ENSP00000456457.1:p.His140Tyr
|
|
ENST00000567034.5:n.886C>T
|
|
|
ENST00000568763.1:n.1730C>T
|
|
|
ENST00000568982.5:n.536C>T
|
|
|
ENST00000569203.5:c.418C>T
|
ENSP00000454752.1:p.His140Tyr
|
|
ENST00000569469.1:n.432-127C>T
|
|
|
ENST00000569970.1:c.418C>T
|
ENSP00000457509.1:p.His140Tyr
|
|
ENST00000570045.5:c.418C>T
|
ENSP00000455552.1:p.His140Tyr
|
|
ENST00000570244.5:c.295C>T
|
ENSP00000457332.1:p.His99Tyr
|
|
NM_001193333.2:c.418C>T
|
NP_001180262.1:p.His140Tyr
|
|
NM_007074.3:c.418C>T
|
NP_009005.1:p.His140Tyr
|
|
XM_011545714.1:c.418C>T
|
XP_011544016.1:p.His140Tyr
|
|
XM_011545714.2:c.418C>T
|
XP_011544016.1:p.His140Tyr
|
|
XM_017022885.2:c.418C>T
|
XP_016878374.1:p.His140Tyr
|
|
XM_017022886.1:c.418C>T
|
XP_016878375.1:p.His140Tyr
|
|
NM_007074.4:c.418C>T
MANE Select
|
NP_009005.1:p.His140Tyr
|
|
NM_001193333.3:c.418C>T
|
NP_001180262.1:p.His140Tyr
|
|