ENST00000356392.9:c.1136T>G
MANE Select
|
ENSP00000348757.3:p.Leu379Arg
|
|
ENST00000356392.8:c.1136T>G
|
ENSP00000348757.3:p.Leu379Arg
|
|
ENST00000586836.5:c.563T>G
|
ENSP00000467429.1:p.Leu188Arg
|
|
ENST00000591179.5:c.956T>G
|
ENSP00000466800.1:p.Leu319Arg
|
|
ENST00000591345.5:c.*1055T>G
|
ENSP00000467313.1:n.*1055T>G
|
|
NM_001302453.1:c.974T>G
|
NP_001289382.1:p.Leu325Arg
|
|
NM_001302454.1:c.956T>G
|
NP_001289383.1:p.Leu319Arg
|
|
NM_145045.4:c.1136T>G
|
NP_659482.3:p.Leu379Arg
|
|
XM_017026241.1:c.*30T>G
|
XP_016881730.1:n.*30T>G
|
|
NM_145045.5:c.1136T>G
MANE Select
|
NP_659482.3:p.Leu379Arg
|
|
NM_001302454.2:c.956T>G
|
NP_001289383.1:p.Leu319Arg
|
|