|
ENST00000368336.10:c.718G>T
MANE Select
|
ENSP00000357320.5:p.Val240Phe
|
|
|
ENST00000343043.7:c.718G>T
|
ENSP00000341692.3:p.Val240Phe
|
|
|
ENST00000368336.9:c.718G>T
|
ENSP00000357320.5:p.Val240Phe
|
|
|
ENST00000421487.6:c.616G>T
|
ENSP00000412605.2:p.Val206Phe
|
|
|
ENST00000462978.1:n.246G>T
|
|
|
|
ENST00000463575.5:c.493G>T
|
ENSP00000476291.1:p.Val165Phe
|
|
|
ENST00000466384.5:n.353G>T
|
|
|
|
ENST00000471214.5:c.718G>T
|
ENSP00000476899.1:p.Val240Phe
|
|
|
ENST00000471642.6:c.595G>T
|
ENSP00000476592.1:p.Val199Phe
|
|
|
ENST00000475056.5:c.34G>T
|
ENSP00000476624.1:p.Val12Phe
|
|
|
ENST00000477394.5:c.66G>T
|
|
|
|
ENST00000479151.5:c.450G>T
|
|
|
|
ENST00000490249.5:c.34G>T
|
ENSP00000477139.1:p.Val12Phe
|
|
|
ENST00000497826.5:c.544G>T
|
ENSP00000476840.1:p.Val182Phe
|
|
|
ENST00000535183.5:c.595G>T
|
ENSP00000445003.1:p.Val199Phe
|
|
|
NM_001199849.1:c.718G>T
|
NP_001186778.1:p.Val240Phe
|
|
|
NM_001199850.1:c.616G>T
|
NP_001186779.1:p.Val206Phe
|
|
|
NM_001199851.1:c.595G>T
|
NP_001186780.1:p.Val199Phe
|
|
|
NM_004632.3:c.718G>T
|
NP_004623.1:p.Val240Phe
|
|
|
NM_033657.2:c.718G>T
|
NP_387506.1:p.Val240Phe
|
|
|
XM_005245480.2:c.616G>T
|
XP_005245537.1:p.Val206Phe
|
|
|
XM_005245481.2:c.595G>T
|
XP_005245538.1:p.Val199Phe
|
|
|
XM_005245482.3:c.493G>T
|
XP_005245539.1:p.Val165Phe
|
|
|
XM_011509972.1:c.637G>T
|
XP_011508274.1:p.Val213Phe
|
|
|
XM_017002289.1:c.637G>T
|
XP_016857778.1:p.Val213Phe
|
|
|
XM_017002290.1:c.637G>T
|
XP_016857779.1:p.Val213Phe
|
|
|
XM_017002291.1:c.616G>T
|
XP_016857780.1:p.Val206Phe
|
|
|
XM_017002292.1:c.595G>T
|
XP_016857781.1:p.Val199Phe
|
|
|
XM_017002293.1:c.595G>T
|
XP_016857782.1:p.Val199Phe
|
|
|
XM_017002294.1:c.535G>T
|
XP_016857783.1:p.Val179Phe
|
|
|
XM_017002295.1:c.514G>T
|
XP_016857784.1:p.Val172Phe
|
|
|
XM_024449697.1:c.718G>T
|
XP_024305465.1:p.Val240Phe
|
|
|
XM_024449698.1:c.637G>T
|
XP_024305466.1:p.Val213Phe
|
|
|
XM_024449700.1:c.514G>T
|
XP_024305468.1:p.Val172Phe
|
|
|
NM_004632.4:c.718G>T
MANE Select
|
NP_004623.1:p.Val240Phe
|
|
