ENST00000356392.9:c.848T>G
MANE Select
|
ENSP00000348757.3:p.Leu283Arg
|
|
ENST00000356392.8:c.848T>G
|
ENSP00000348757.3:p.Leu283Arg
|
|
ENST00000586836.5:c.275T>G
|
ENSP00000467429.1:p.Leu92Arg
|
|
ENST00000591179.5:c.668T>G
|
ENSP00000466800.1:p.Leu223Arg
|
|
ENST00000591345.5:c.*767T>G
|
ENSP00000467313.1:n.*767T>G
|
|
NM_001302453.1:c.686T>G
|
NP_001289382.1:p.Leu229Arg
|
|
NM_001302454.1:c.668T>G
|
NP_001289383.1:p.Leu223Arg
|
|
NM_145045.4:c.848T>G
|
NP_659482.3:p.Leu283Arg
|
|
XM_017026241.1:c.848T>G
|
XP_016881730.1:p.Leu283Arg
|
|
NM_145045.5:c.848T>G
MANE Select
|
NP_659482.3:p.Leu283Arg
|
|
NM_001302454.2:c.668T>G
|
NP_001289383.1:p.Leu223Arg
|
|