ENST00000403733.8:c.3189G>C
MANE Select
|
ENSP00000384222.3:p.Val1063=
|
|
ENST00000403733.7:c.3189G>C
|
ENSP00000384222.3:p.Val1063=
|
|
ENST00000427431.5:c.*2581G>C
|
ENSP00000393342.1:n.*2581G>C
|
|
ENST00000438543.5:c.*985G>C
|
ENSP00000413521.1:n.*985G>C
|
|
ENST00000448232.6:c.3261G>C
|
ENSP00000398577.2:p.Val1087=
|
|
ENST00000504005.5:c.2235G>C
|
ENSP00000427569.1:p.Val745=
|
|
ENST00000508747.1:c.573G>C
|
ENSP00000420835.1:p.Val191=
|
|
ENST00000513834.5:c.3042G>C
|
ENSP00000425054.1:p.Val1014=
|
|
NM_024949.5:c.3189G>C
|
NP_079225.5:p.Val1063=
|
|
XM_011532269.1:c.3261G>C
|
XP_011530571.1:p.Val1087=
|
|
XM_011532269.3:c.3261G>C
|
XP_011530571.1:p.Val1087=
|
|
XM_024454225.1:c.2967G>C
|
XP_024309993.1:p.Val989=
|
|
NM_024949.6:c.3189G>C
MANE Select
|
NP_079225.5:p.Val1063=
|
|