ENST00000356392.9:c.1148A>T
MANE Select
|
ENSP00000348757.3:p.Asp383Val
|
|
ENST00000356392.8:c.1148A>T
|
ENSP00000348757.3:p.Asp383Val
|
|
ENST00000586836.5:c.575A>T
|
ENSP00000467429.1:p.Asp192Val
|
|
ENST00000591179.5:c.968A>T
|
ENSP00000466800.1:p.Asp323Val
|
|
ENST00000591345.5:c.*1067A>T
|
ENSP00000467313.1:n.*1067A>T
|
|
NM_001302453.1:c.986A>T
|
NP_001289382.1:p.Asp329Val
|
|
NM_001302454.1:c.968A>T
|
NP_001289383.1:p.Asp323Val
|
|
NM_145045.4:c.1148A>T
|
NP_659482.3:p.Asp383Val
|
|
XM_017026241.1:c.*42A>T
|
XP_016881730.1:n.*42A>T
|
|
NM_145045.5:c.1148A>T
MANE Select
|
NP_659482.3:p.Asp383Val
|
|
NM_001302454.2:c.968A>T
|
NP_001289383.1:p.Asp323Val
|
|