ENST00000356392.9:c.923C>A
MANE Select
|
ENSP00000348757.3:p.Ala308Asp
|
|
ENST00000356392.8:c.923C>A
|
ENSP00000348757.3:p.Ala308Asp
|
|
ENST00000586836.5:c.350C>A
|
ENSP00000467429.1:p.Ala117Asp
|
|
ENST00000591179.5:c.743C>A
|
ENSP00000466800.1:p.Ala248Asp
|
|
ENST00000591345.5:c.*842C>A
|
ENSP00000467313.1:n.*842C>A
|
|
NM_001302453.1:c.761C>A
|
NP_001289382.1:p.Ala254Asp
|
|
NM_001302454.1:c.743C>A
|
NP_001289383.1:p.Ala248Asp
|
|
NM_145045.4:c.923C>A
|
NP_659482.3:p.Ala308Asp
|
|
XM_017026241.1:c.904+19C>A
|
XP_016881730.1:n.904+19C>A
|
|
NM_145045.5:c.923C>A
MANE Select
|
NP_659482.3:p.Ala308Asp
|
|
NM_001302454.2:c.743C>A
|
NP_001289383.1:p.Ala248Asp
|
|