ENST00000547103.7:c.6115T>C
MANE Select
|
ENSP00000447211.2:p.Tyr2039His
|
|
ENST00000642294.1:c.55T>C
|
ENSP00000493572.1:p.Tyr19His
|
|
ENST00000646859.1:c.5980T>C
|
ENSP00000496036.1:p.Tyr1994His
|
|
ENST00000298820.7:c.1416T>C
|
|
|
ENST00000458043.6:c.6088T>C
|
ENSP00000400895.2:p.Tyr2030His
|
|
ENST00000546620.5:n.371T>C
|
|
|
ENST00000547103.5:c.6052T>C
|
ENSP00000447211.1:p.Tyr2018His
|
|
ENST00000550182.2:c.139T>C
|
ENSP00000449641.1:p.Tyr47His
|
|
ENST00000551340.5:c.243T>C
|
|
|
NM_173591.3:c.6088T>C
|
NP_775862.3:p.Tyr2030His
|
|
XM_005268802.2:c.6139T>C
|
XP_005268859.1:p.Tyr2047His
|
|
XM_011538191.1:c.6139T>C
|
XP_011536493.1:p.Tyr2047His
|
|
XM_011538192.1:c.5986T>C
|
XP_011536494.1:p.Tyr1996His
|
|
XM_011538193.1:c.5773T>C
|
XP_011536495.1:p.Tyr1925His
|
|
XM_005268802.3:c.6139T>C
|
XP_005268859.1:p.Tyr2047His
|
|
XM_011538192.2:c.5986T>C
|
XP_011536494.1:p.Tyr1996His
|
|
NM_001368062.1:c.5953T>C
|
NP_001354991.1:p.Tyr1985His
|
|
NM_001368062.3:c.5980T>C
|
NP_001354991.2:p.Tyr1994His
|
|
NM_001378609.3:c.6115T>C
MANE Select
|
NP_001365538.2:p.Tyr2039His
|
|
NM_001378610.3:c.6115T>C
|
NP_001365539.2:p.Tyr2039His
|
|
NM_173591.7:c.6115T>C
|
NP_775862.4:p.Tyr2039His
|
|