ENST00000356392.9:c.1138G>T
MANE Select
|
ENSP00000348757.3:p.Ala380Ser
|
|
ENST00000356392.8:c.1138G>T
|
ENSP00000348757.3:p.Ala380Ser
|
|
ENST00000586836.5:c.565G>T
|
ENSP00000467429.1:p.Ala189Ser
|
|
ENST00000591179.5:c.958G>T
|
ENSP00000466800.1:p.Ala320Ser
|
|
ENST00000591345.5:c.*1057G>T
|
ENSP00000467313.1:n.*1057G>T
|
|
NM_001302453.1:c.976G>T
|
NP_001289382.1:p.Ala326Ser
|
|
NM_001302454.1:c.958G>T
|
NP_001289383.1:p.Ala320Ser
|
|
NM_145045.4:c.1138G>T
|
NP_659482.3:p.Ala380Ser
|
|
XM_017026241.1:c.*32G>T
|
XP_016881730.1:n.*32G>T
|
|
NM_145045.5:c.1138G>T
MANE Select
|
NP_659482.3:p.Ala380Ser
|
|
NM_001302454.2:c.958G>T
|
NP_001289383.1:p.Ala320Ser
|
|