ENST00000432791.7:c.2843A>T
MANE Select
|
ENSP00000387393.3:p.Tyr948Phe
|
|
ENST00000572904.6:c.2843A>T
|
ENSP00000461484.1:p.Tyr948Phe
|
|
ENST00000574590.6:c.2840A>T
|
ENSP00000461812.2:p.Tyr947Phe
|
|
ENST00000575318.6:c.2651A>T
|
ENSP00000461299.1:p.Tyr884Phe
|
|
ENST00000638275.1:c.2651A>T
|
ENSP00000492576.1:p.Tyr884Phe
|
|
ENST00000638291.1:n.671A>T
|
|
|
ENST00000638551.1:n.791A>T
|
|
|
ENST00000639467.1:c.500A>T
|
ENSP00000492741.1:p.Tyr167Phe
|
|
ENST00000639531.1:c.2654A>T
|
ENSP00000491765.1:p.Tyr885Phe
|
|
ENST00000639805.1:n.260A>T
|
|
|
ENST00000640751.1:n.438A>T
|
|
|
ENST00000648792.1:c.2838-127A>T
|
ENSP00000497628.1:n.2838-127A>T
|
|
ENST00000262419.10:c.2843A>T
|
ENSP00000262419.6:p.Tyr948Phe
|
|
ENST00000432791.5:c.2840A>T
|
ENSP00000387393.2:p.Tyr947Phe
|
|
ENST00000572218.5:n.7060A>T
|
|
|
ENST00000572904.5:c.2843A>T
|
ENSP00000461484.1:p.Tyr948Phe
|
|
ENST00000573682.1:n.229A>T
|
|
|
ENST00000574590.5:c.2843A>T
|
ENSP00000461812.1:p.Tyr948Phe
|
|
ENST00000574963.1:n.273A>T
|
|
|
ENST00000575318.5:c.2651A>T
|
ENSP00000461299.1:p.Tyr884Phe
|
|
ENST00000576870.5:n.815A>T
|
|
|
NM_001193465.1:c.2840A>T
|
NP_001180394.1:p.Tyr947Phe
|
|
NM_001193466.1:c.2843A>T
|
NP_001180395.1:p.Tyr948Phe
|
|
NM_015443.3:c.2843A>T
|
NP_056258.1:p.Tyr948Phe
|
|
XM_006721823.1:c.2843A>T
|
XP_006721886.1:p.Tyr948Phe
|
|
XM_006721824.2:c.2843A>T
|
XP_006721887.1:p.Tyr948Phe
|
|
XM_011524628.1:c.2840A>T
|
XP_011522930.1:p.Tyr947Phe
|
|
XM_011524629.1:c.2741A>T
|
XP_011522931.1:p.Tyr914Phe
|
|
XM_011524630.1:c.2654A>T
|
XP_011522932.1:p.Tyr885Phe
|
|
XM_011524631.1:c.2651A>T
|
XP_011522933.1:p.Tyr884Phe
|
|
XM_011524632.1:c.1613A>T
|
XP_011522934.1:p.Tyr538Phe
|
|
XM_006721823.2:c.2843A>T
|
XP_006721886.1:p.Tyr948Phe
|
|
XM_006721824.4:c.2843A>T
|
XP_006721887.1:p.Tyr948Phe
|
|
XM_011524628.3:c.2840A>T
|
XP_011522930.1:p.Tyr947Phe
|
|
XM_011524629.3:c.2741A>T
|
XP_011522931.1:p.Tyr914Phe
|
|
XM_011524630.3:c.2654A>T
|
XP_011522932.1:p.Tyr885Phe
|
|
XM_011524631.3:c.2651A>T
|
XP_011522933.1:p.Tyr884Phe
|
|
XM_011524632.3:c.1613A>T
|
XP_011522934.1:p.Tyr538Phe
|
|
XM_017024488.2:c.2651A>T
|
XP_016879977.1:p.Tyr884Phe
|
|
NM_001193466.2:c.2843A>T
|
NP_001180395.1:p.Tyr948Phe
|
|
NM_015443.4:c.2843A>T
MANE Select
|
NP_056258.1:p.Tyr948Phe
|
|
NM_001193465.2:c.2840A>T
|
NP_001180394.1:p.Tyr947Phe
|
|
NM_001379198.1:c.2843A>T
|
NP_001366127.1:p.Tyr948Phe
|
|