ENST00000403733.8:c.3188T>C
MANE Select
|
ENSP00000384222.3:p.Val1063Ala
|
|
ENST00000403733.7:c.3188T>C
|
ENSP00000384222.3:p.Val1063Ala
|
|
ENST00000427431.5:c.*2580T>C
|
ENSP00000393342.1:n.*2580T>C
|
|
ENST00000438543.5:c.*984T>C
|
ENSP00000413521.1:n.*984T>C
|
|
ENST00000448232.6:c.3260T>C
|
ENSP00000398577.2:p.Val1087Ala
|
|
ENST00000504005.5:c.2234T>C
|
ENSP00000427569.1:p.Val745Ala
|
|
ENST00000508747.1:c.572T>C
|
ENSP00000420835.1:p.Val191Ala
|
|
ENST00000513834.5:c.3041T>C
|
ENSP00000425054.1:p.Val1014Ala
|
|
NM_024949.5:c.3188T>C
|
NP_079225.5:p.Val1063Ala
|
|
XM_011532269.1:c.3260T>C
|
XP_011530571.1:p.Val1087Ala
|
|
XM_011532269.3:c.3260T>C
|
XP_011530571.1:p.Val1087Ala
|
|
XM_024454225.1:c.2966T>C
|
XP_024309993.1:p.Val989Ala
|
|
NM_024949.6:c.3188T>C
MANE Select
|
NP_079225.5:p.Val1063Ala
|
|