ENST00000651671.1:c.6527T>A
MANE Select
|
ENSP00000498587.1:p.Leu2176His
|
|
ENST00000679595.1:c.*1567T>A
|
ENSP00000506241.1:n.*1567T>A
|
|
ENST00000679969.1:n.3123T>A
|
|
|
ENST00000680003.1:n.2859T>A
|
|
|
ENST00000680133.1:c.6413T>A
|
ENSP00000505319.1:p.Leu2138His
|
|
ENST00000680218.1:c.6407T>A
|
ENSP00000505339.1:p.Leu2136His
|
|
ENST00000680668.1:c.6413T>A
|
ENSP00000506336.1:p.Leu2138His
|
|
ENST00000680778.1:c.4124T>A
|
ENSP00000506033.1:p.Leu1375His
|
|
ENST00000680924.1:c.*3927T>A
|
ENSP00000506031.1:n.*3927T>A
|
|
ENST00000681135.1:c.*4136T>A
|
ENSP00000506636.1:n.*4136T>A
|
|
ENST00000681298.1:n.4632T>A
|
|
|
ENST00000681454.1:c.*5763T>A
|
ENSP00000505763.1:n.*5763T>A
|
|
ENST00000277541.6:c.6527T>A
|
ENSP00000277541.6:p.Leu2176His
|
|
NM_017617.3:c.6527T>A
|
NP_060087.3:p.Leu2176His
|
|
XM_011518717.1:c.5828T>A
|
XP_011517019.1:p.Leu1943His
|
|
NM_017617.5:c.6527T>A
MANE Select
|
NP_060087.3:p.Leu2176His
|
|
XM_011518717.2:c.5804T>A
|
XP_011517019.2:p.Leu1935His
|
|