ENST00000356392.9:c.1159C>G
MANE Select
|
ENSP00000348757.3:p.Gln387Glu
|
|
ENST00000356392.8:c.1159C>G
|
ENSP00000348757.3:p.Gln387Glu
|
|
ENST00000586836.5:c.586C>G
|
ENSP00000467429.1:p.Gln196Glu
|
|
ENST00000591179.5:c.979C>G
|
ENSP00000466800.1:p.Gln327Glu
|
|
ENST00000591345.5:c.*1078C>G
|
ENSP00000467313.1:n.*1078C>G
|
|
NM_001302453.1:c.997C>G
|
NP_001289382.1:p.Gln333Glu
|
|
NM_001302454.1:c.979C>G
|
NP_001289383.1:p.Gln327Glu
|
|
NM_145045.4:c.1159C>G
|
NP_659482.3:p.Gln387Glu
|
|
XM_017026241.1:c.*53C>G
|
XP_016881730.1:n.*53C>G
|
|
NM_145045.5:c.1159C>G
MANE Select
|
NP_659482.3:p.Gln387Glu
|
|
NM_001302454.2:c.979C>G
|
NP_001289383.1:p.Gln327Glu
|
|