ENST00000356392.9:c.1124T>A
MANE Select
|
ENSP00000348757.3:p.Val375Glu
|
|
ENST00000356392.8:c.1124T>A
|
ENSP00000348757.3:p.Val375Glu
|
|
ENST00000586836.5:c.551T>A
|
ENSP00000467429.1:p.Val184Glu
|
|
ENST00000591179.5:c.944T>A
|
ENSP00000466800.1:p.Val315Glu
|
|
ENST00000591345.5:c.*1043T>A
|
ENSP00000467313.1:n.*1043T>A
|
|
NM_001302453.1:c.962T>A
|
NP_001289382.1:p.Val321Glu
|
|
NM_001302454.1:c.944T>A
|
NP_001289383.1:p.Val315Glu
|
|
NM_145045.4:c.1124T>A
|
NP_659482.3:p.Val375Glu
|
|
XM_017026241.1:c.*18T>A
|
XP_016881730.1:n.*18T>A
|
|
NM_145045.5:c.1124T>A
MANE Select
|
NP_659482.3:p.Val375Glu
|
|
NM_001302454.2:c.944T>A
|
NP_001289383.1:p.Val315Glu
|
|