ENST00000356392.9:c.1179C>G
MANE Select
|
ENSP00000348757.3:p.Ser393Arg
|
|
ENST00000356392.8:c.1179C>G
|
ENSP00000348757.3:p.Ser393Arg
|
|
ENST00000586836.5:c.606C>G
|
ENSP00000467429.1:p.Ser202Arg
|
|
ENST00000591179.5:c.999C>G
|
ENSP00000466800.1:p.Ser333Arg
|
|
ENST00000591345.5:c.*1098C>G
|
ENSP00000467313.1:n.*1098C>G
|
|
NM_001302453.1:c.1017C>G
|
NP_001289382.1:p.Ser339Arg
|
|
NM_001302454.1:c.999C>G
|
NP_001289383.1:p.Ser333Arg
|
|
NM_145045.4:c.1179C>G
|
NP_659482.3:p.Ser393Arg
|
|
XM_017026241.1:c.*73C>G
|
XP_016881730.1:n.*73C>G
|
|
NM_145045.5:c.1179C>G
MANE Select
|
NP_659482.3:p.Ser393Arg
|
|
NM_001302454.2:c.999C>G
|
NP_001289383.1:p.Ser333Arg
|
|