ENST00000356392.9:c.1247T>A
MANE Select
|
ENSP00000348757.3:p.Leu416His
|
|
ENST00000356392.8:c.1247T>A
|
ENSP00000348757.3:p.Leu416His
|
|
ENST00000586836.5:c.674T>A
|
ENSP00000467429.1:p.Leu225His
|
|
ENST00000591179.5:c.1067T>A
|
ENSP00000466800.1:p.Leu356His
|
|
ENST00000591345.5:c.*1166T>A
|
ENSP00000467313.1:n.*1166T>A
|
|
NM_001302453.1:c.1085T>A
|
NP_001289382.1:p.Leu362His
|
|
NM_001302454.1:c.1067T>A
|
NP_001289383.1:p.Leu356His
|
|
NM_145045.4:c.1247T>A
|
NP_659482.3:p.Leu416His
|
|
NM_145045.5:c.1247T>A
MANE Select
|
NP_659482.3:p.Leu416His
|
|
NM_001302454.2:c.1067T>A
|
NP_001289383.1:p.Leu356His
|
|