ENST00000356392.9:c.906T>C
MANE Select
|
ENSP00000348757.3:p.Ser302=
|
|
ENST00000356392.8:c.906T>C
|
ENSP00000348757.3:p.Ser302=
|
|
ENST00000586836.5:c.333T>C
|
ENSP00000467429.1:p.Ser111=
|
|
ENST00000591179.5:c.726T>C
|
ENSP00000466800.1:p.Ser242=
|
|
ENST00000591345.5:c.*825T>C
|
ENSP00000467313.1:n.*825T>C
|
|
NM_001302453.1:c.744T>C
|
NP_001289382.1:p.Ser248=
|
|
NM_001302454.1:c.726T>C
|
NP_001289383.1:p.Ser242=
|
|
NM_145045.4:c.906T>C
|
NP_659482.3:p.Ser302=
|
|
XM_017026241.1:c.904+2T>C
|
XP_016881730.1:n.904+2T>C
|
|
NM_145045.5:c.906T>C
MANE Select
|
NP_659482.3:p.Ser302=
|
|
NM_001302454.2:c.726T>C
|
NP_001289383.1:p.Ser242=
|
|