ENST00000547103.7:c.6119G>T
MANE Select
|
ENSP00000447211.2:p.Cys2040Phe
|
|
ENST00000642294.1:c.59G>T
|
ENSP00000493572.1:p.Cys20Phe
|
|
ENST00000646859.1:c.5984G>T
|
ENSP00000496036.1:p.Cys1995Phe
|
|
ENST00000298820.7:c.1420G>T
|
|
|
ENST00000458043.6:c.6092G>T
|
ENSP00000400895.2:p.Cys2031Phe
|
|
ENST00000546620.5:n.375G>T
|
|
|
ENST00000547103.5:c.6056G>T
|
ENSP00000447211.1:p.Cys2019Phe
|
|
ENST00000550182.2:c.143G>T
|
ENSP00000449641.1:p.Cys48Phe
|
|
ENST00000551340.5:c.247G>T
|
|
|
NM_173591.3:c.6092G>T
|
NP_775862.3:p.Cys2031Phe
|
|
XM_005268802.2:c.6143G>T
|
XP_005268859.1:p.Cys2048Phe
|
|
XM_011538191.1:c.6143G>T
|
XP_011536493.1:p.Cys2048Phe
|
|
XM_011538192.1:c.5990G>T
|
XP_011536494.1:p.Cys1997Phe
|
|
XM_011538193.1:c.5777G>T
|
XP_011536495.1:p.Cys1926Phe
|
|
XM_005268802.3:c.6143G>T
|
XP_005268859.1:p.Cys2048Phe
|
|
XM_011538192.2:c.5990G>T
|
XP_011536494.1:p.Cys1997Phe
|
|
NM_001368062.1:c.5957G>T
|
NP_001354991.1:p.Cys1986Phe
|
|
NM_001368062.3:c.5984G>T
|
NP_001354991.2:p.Cys1995Phe
|
|
NM_001378609.3:c.6119G>T
MANE Select
|
NP_001365538.2:p.Cys2040Phe
|
|
NM_001378610.3:c.6119G>T
|
NP_001365539.2:p.Cys2040Phe
|
|
NM_173591.7:c.6119G>T
|
NP_775862.4:p.Cys2040Phe
|
|