ENST00000356392.9:c.1118C>A
MANE Select
|
ENSP00000348757.3:p.Ser373Ter
|
|
ENST00000356392.8:c.1118C>A
|
ENSP00000348757.3:p.Ser373Ter
|
|
ENST00000586836.5:c.545C>A
|
ENSP00000467429.1:p.Ser182Ter
|
|
ENST00000591179.5:c.938C>A
|
ENSP00000466800.1:p.Ser313Ter
|
|
ENST00000591345.5:c.*1037C>A
|
ENSP00000467313.1:n.*1037C>A
|
|
NM_001302453.1:c.956C>A
|
NP_001289382.1:p.Ser319Ter
|
|
NM_001302454.1:c.938C>A
|
NP_001289383.1:p.Ser313Ter
|
|
NM_145045.4:c.1118C>A
|
NP_659482.3:p.Ser373Ter
|
|
XM_017026241.1:c.*12C>A
|
XP_016881730.1:n.*12C>A
|
|
NM_145045.5:c.1118C>A
MANE Select
|
NP_659482.3:p.Ser373Ter
|
|
NM_001302454.2:c.938C>A
|
NP_001289383.1:p.Ser313Ter
|
|