ENST00000428695.6:c.691G>T
|
ENSP00000388581.1:p.Val231Phe
|
|
ENST00000700191.1:c.691G>T
|
ENSP00000514853.1:p.Val231Phe
|
|
ENST00000700193.1:c.1045G>T
|
ENSP00000514854.1:p.Val349Phe
|
|
ENST00000700208.1:c.347-76157G>T
|
ENSP00000514860.1:n.347-76157G>T
|
|
ENST00000700210.1:c.699G>T
|
|
|
ENST00000417098.6:c.1045G>T
MANE Select
|
ENSP00000401112.1:p.Val349Phe
|
|
ENST00000260926.9:c.1045G>T
|
ENSP00000260926.5:p.Val349Phe
|
|
ENST00000417098.5:c.1045G>T
|
ENSP00000401112.1:p.Val349Phe
|
|
ENST00000428695.5:c.691G>T
|
ENSP00000388581.1:p.Val231Phe
|
|
ENST00000443023.5:c.868G>T
|
ENSP00000388764.1:p.Val290Phe
|
|
ENST00000457245.5:c.1045G>T
|
ENSP00000405420.1:p.Val349Phe
|
|
ENST00000483346.2:n.684G>T
|
|
|
ENST00000614512.4:c.691G>T
|
ENSP00000483287.1:p.Val231Phe
|
|
NM_001172509.1:c.1045G>T
|
NP_001165980.1:p.Val349Phe
|
|
NM_001172517.1:c.1045G>T
|
NP_001165988.1:p.Val349Phe
|
|
NM_015265.3:c.1045G>T
|
NP_056080.1:p.Val349Phe
|
|
XM_005246396.1:c.871G>T
|
XP_005246453.1:p.Val291Phe
|
|
XM_006712372.1:c.1045G>T
|
XP_006712435.1:p.Val349Phe
|
|
XM_011510840.1:c.1045G>T
|
XP_011509142.1:p.Val349Phe
|
|
XM_005246396.3:c.871G>T
|
XP_005246453.1:p.Val291Phe
|
|
XM_011510840.3:c.1045G>T
|
XP_011509142.1:p.Val349Phe
|
|
XM_017003656.1:c.871G>T
|
XP_016859145.1:p.Val291Phe
|
|
XM_024452767.1:c.622G>T
|
XP_024308535.1:p.Val208Phe
|
|
XM_024452768.1:c.622G>T
|
XP_024308536.1:p.Val208Phe
|
|
NM_001172509.2:c.1045G>T
MANE Select
|
NP_001165980.1:p.Val349Phe
|
|
NM_015265.4:c.1045G>T
|
NP_056080.1:p.Val349Phe
|
|