ENST00000426333.7:c.171G=
MANE Select
|
ENSP00000392094.1:p.Val57=
|
|
ENST00000402521.7:c.66G=
|
ENSP00000385873.2:p.Val22=
|
|
ENST00000426333.6:c.171G=
|
ENSP00000392094.1:p.Val57=
|
|
ENST00000588374.1:c.82-1351G=
|
ENSP00000467639.1:n.82-1351G=
|
|
ENST00000589211.1:n.562G=
|
|
|
ENST00000589825.5:n.252G=
|
|
|
ENST00000591382.5:c.171G=
|
ENSP00000467805.1:p.Val57=
|
|
ENST00000592408.5:n.382G=
|
|
|
ENST00000592576.5:c.171G=
|
ENSP00000465058.1:p.Val57=
|
|
ENST00000592701.2:c.171G=
|
ENSP00000464908.1:p.Val57=
|
|
ENST00000593072.5:c.171G=
|
ENSP00000464882.1:p.Val57=
|
|
NM_001142605.1:c.66G=
|
NP_001136077.1:p.Val22=
|
|
NM_001258353.1:c.171G=
|
NP_001245282.1:p.Val57=
|
|
NM_001258354.1:c.171G=
|
NP_001245283.1:p.Val57=
|
|
NM_004247.3:c.171G=
|
NP_004238.3:p.Val57=
|
|
XR_934602.1:n.256G=
|
|
|
XR_934602.3:n.252G=
|
|
|
NM_004247.4:c.171G=
MANE Select
|
NP_004238.3:p.Val57=
|
|
NM_001142605.2:c.66G=
|
NP_001136077.1:p.Val22=
|
|
NM_001258353.2:c.171G=
|
NP_001245282.1:p.Val57=
|
|
NM_001258354.2:c.171G=
|
NP_001245283.1:p.Val57=
|
|