ENST00000240651.14:c.319T>C
MANE Select
|
ENSP00000240651.9:p.Tyr107His
|
|
ENST00000240651.13:c.319T>C
|
ENSP00000240651.9:p.Tyr107His
|
|
ENST00000375266.8:c.*245T>C
|
ENSP00000364415.4:n.*245T>C
|
|
ENST00000538582.5:c.106T>C
|
ENSP00000438505.1:p.Tyr36His
|
|
ENST00000543476.5:c.319T>C
|
ENSP00000440192.1:p.Tyr107His
|
|
ENST00000544970.5:c.319T>C
|
ENSP00000439106.1:p.Tyr107His
|
|
NM_024854.3:c.319T>C
|
NP_079130.2:p.Tyr107His
|
|
XM_006719153.2:c.319T>C
|
XP_006719216.1:p.Tyr107His
|
|
XR_242902.3:n.446T>C
|
|
|
NM_001350912.1:c.106T>C
|
NP_001337841.1:p.Tyr36His
|
|
NM_001350913.1:c.-385T>C
|
NP_001337842.1:n.-385T>C
|
|
NM_024854.4:c.319T>C
|
NP_079130.2:p.Tyr107His
|
|
XM_006719153.3:c.319T>C
|
XP_006719216.1:p.Tyr107His
|
|
XR_242902.4:n.420T>C
|
|
|
NM_024854.5:c.319T>C
MANE Select
|
NP_079130.2:p.Tyr107His
|
|
NM_001350913.2:c.-385T>C
|
NP_001337842.1:n.-385T>C
|
|
NM_001350912.2:c.106T>C
|
NP_001337841.1:p.Tyr36His
|
|