ENST00000651671.1:c.6140T>A
MANE Select
|
ENSP00000498587.1:p.Leu2047His
|
|
ENST00000679595.1:c.*1180T>A
|
ENSP00000506241.1:n.*1180T>A
|
|
ENST00000679969.1:n.2736T>A
|
|
|
ENST00000680003.1:n.2472T>A
|
|
|
ENST00000680133.1:c.6026T>A
|
ENSP00000505319.1:p.Leu2009His
|
|
ENST00000680218.1:c.6020T>A
|
ENSP00000505339.1:p.Leu2007His
|
|
ENST00000680668.1:c.6026T>A
|
ENSP00000506336.1:p.Leu2009His
|
|
ENST00000680778.1:c.3737T>A
|
ENSP00000506033.1:p.Leu1246His
|
|
ENST00000680924.1:c.*3540T>A
|
ENSP00000506031.1:n.*3540T>A
|
|
ENST00000681135.1:c.*3749T>A
|
ENSP00000506636.1:n.*3749T>A
|
|
ENST00000681298.1:n.4245T>A
|
|
|
ENST00000681454.1:c.*5376T>A
|
ENSP00000505763.1:n.*5376T>A
|
|
ENST00000277541.6:c.6140T>A
|
ENSP00000277541.6:p.Leu2047His
|
|
NM_017617.3:c.6140T>A
|
NP_060087.3:p.Leu2047His
|
|
XM_011518717.1:c.5441T>A
|
XP_011517019.1:p.Leu1814His
|
|
NM_017617.5:c.6140T>A
MANE Select
|
NP_060087.3:p.Leu2047His
|
|
XM_011518717.2:c.5417T>A
|
XP_011517019.2:p.Leu1806His
|
|