ENST00000403733.8:c.3227C>T
MANE Select
|
ENSP00000384222.3:p.Ser1076Phe
|
|
ENST00000403733.7:c.3227C>T
|
ENSP00000384222.3:p.Ser1076Phe
|
|
ENST00000427431.5:c.*2619C>T
|
ENSP00000393342.1:n.*2619C>T
|
|
ENST00000438543.5:c.*1023C>T
|
ENSP00000413521.1:n.*1023C>T
|
|
ENST00000448232.6:c.3299C>T
|
ENSP00000398577.2:p.Ser1100Phe
|
|
ENST00000504005.5:c.2273C>T
|
ENSP00000427569.1:p.Ser758Phe
|
|
ENST00000508747.1:c.611C>T
|
ENSP00000420835.1:p.Ser204Phe
|
|
ENST00000513834.5:c.3080C>T
|
ENSP00000425054.1:p.Ser1027Phe
|
|
NM_024949.5:c.3227C>T
|
NP_079225.5:p.Ser1076Phe
|
|
XM_011532269.1:c.3299C>T
|
XP_011530571.1:p.Ser1100Phe
|
|
XM_011532269.3:c.3299C>T
|
XP_011530571.1:p.Ser1100Phe
|
|
XM_024454225.1:c.3005C>T
|
XP_024309993.1:p.Ser1002Phe
|
|
NM_024949.6:c.3227C>T
MANE Select
|
NP_079225.5:p.Ser1076Phe
|
|