ENST00000432791.7:c.2883T>A
MANE Select
|
ENSP00000387393.3:p.Ser961Arg
|
|
ENST00000572904.6:c.2883T>A
|
ENSP00000461484.1:p.Ser961Arg
|
|
ENST00000574590.6:c.2880T>A
|
ENSP00000461812.2:p.Ser960Arg
|
|
ENST00000575318.6:c.2691T>A
|
ENSP00000461299.1:p.Ser897Arg
|
|
ENST00000638275.1:c.2691T>A
|
ENSP00000492576.1:p.Ser897Arg
|
|
ENST00000638291.1:n.711T>A
|
|
|
ENST00000638551.1:n.831T>A
|
|
|
ENST00000639467.1:c.540T>A
|
ENSP00000492741.1:p.Ser180Arg
|
|
ENST00000639805.1:n.300T>A
|
|
|
ENST00000648792.1:c.2838-87T>A
|
ENSP00000497628.1:n.2838-87T>A
|
|
ENST00000262419.10:c.2883T>A
|
ENSP00000262419.6:p.Ser961Arg
|
|
ENST00000432791.5:c.2880T>A
|
ENSP00000387393.2:p.Ser960Arg
|
|
ENST00000572218.5:n.7100T>A
|
|
|
ENST00000572904.5:c.2883T>A
|
ENSP00000461484.1:p.Ser961Arg
|
|
ENST00000573682.1:n.269T>A
|
|
|
ENST00000574590.5:c.2883T>A
|
ENSP00000461812.1:p.Ser961Arg
|
|
ENST00000574963.1:n.313T>A
|
|
|
ENST00000575318.5:c.2691T>A
|
ENSP00000461299.1:p.Ser897Arg
|
|
ENST00000576870.5:n.855T>A
|
|
|
NM_001193465.1:c.2880T>A
|
NP_001180394.1:p.Ser960Arg
|
|
NM_001193466.1:c.2883T>A
|
NP_001180395.1:p.Ser961Arg
|
|
NM_015443.3:c.2883T>A
|
NP_056258.1:p.Ser961Arg
|
|
XM_006721823.1:c.2883T>A
|
XP_006721886.1:p.Ser961Arg
|
|
XM_006721824.2:c.2883T>A
|
XP_006721887.1:p.Ser961Arg
|
|
XM_011524628.1:c.2880T>A
|
XP_011522930.1:p.Ser960Arg
|
|
XM_011524629.1:c.2781T>A
|
XP_011522931.1:p.Ser927Arg
|
|
XM_011524630.1:c.2694T>A
|
XP_011522932.1:p.Ser898Arg
|
|
XM_011524631.1:c.2691T>A
|
XP_011522933.1:p.Ser897Arg
|
|
XM_011524632.1:c.1653T>A
|
XP_011522934.1:p.Ser551Arg
|
|
XM_006721823.2:c.2883T>A
|
XP_006721886.1:p.Ser961Arg
|
|
XM_006721824.4:c.2883T>A
|
XP_006721887.1:p.Ser961Arg
|
|
XM_011524628.3:c.2880T>A
|
XP_011522930.1:p.Ser960Arg
|
|
XM_011524629.3:c.2781T>A
|
XP_011522931.1:p.Ser927Arg
|
|
XM_011524630.3:c.2694T>A
|
XP_011522932.1:p.Ser898Arg
|
|
XM_011524631.3:c.2691T>A
|
XP_011522933.1:p.Ser897Arg
|
|
XM_011524632.3:c.1653T>A
|
XP_011522934.1:p.Ser551Arg
|
|
XM_017024488.2:c.2691T>A
|
XP_016879977.1:p.Ser897Arg
|
|
NM_001193466.2:c.2883T>A
|
NP_001180395.1:p.Ser961Arg
|
|
NM_015443.4:c.2883T>A
MANE Select
|
NP_056258.1:p.Ser961Arg
|
|
NM_001193465.2:c.2880T>A
|
NP_001180394.1:p.Ser960Arg
|
|
NM_001379198.1:c.2883T>A
|
NP_001366127.1:p.Ser961Arg
|
|