ENST00000261304.7:c.2043G=
MANE Select
|
ENSP00000261304.2:p.Val681=
|
|
ENST00000261304.6:c.2043G=
|
ENSP00000261304.2:p.Val681=
|
|
ENST00000393568.8:c.1974G=
|
ENSP00000377198.4:p.Val658=
|
|
ENST00000393569.6:c.1965G=
|
ENSP00000377199.2:p.Val655=
|
|
ENST00000544807.6:c.1744-748G=
|
ENSP00000437513.2:n.1744-748G=
|
|
ENST00000555000.5:c.1279-748G=
|
ENSP00000450472.1:n.1279-748G=
|
|
NM_000153.3:c.2043G=
|
NP_000144.2:p.Val681=
|
|
NM_001201401.1:c.1974G=
|
NP_001188330.1:p.Val658=
|
|
NM_001201402.1:c.1965G=
|
NP_001188331.1:p.Val655=
|
|
XM_011536618.1:c.1875G=
|
XP_011534920.1:p.Val625=
|
|
XM_011536618.2:c.1875G=
|
XP_011534920.1:p.Val625=
|
|
NM_000153.4:c.2043G=
MANE Select
|
NP_000144.2:p.Val681=
|
|
NM_001201401.2:c.1974G=
|
NP_001188330.1:p.Val658=
|
|
NM_001201402.2:c.1965G=
|
NP_001188331.1:p.Val655=
|
|