ENST00000682422.1:n.809G>A
|
|
|
ENST00000682545.1:c.*234G>A
|
ENSP00000508402.1:n.*234G>A
|
|
ENST00000682887.1:c.1629G>A
|
ENSP00000506946.1:n.1629G>A
|
|
ENST00000683302.1:c.1159G>A
|
ENSP00000507885.1:p.Ala387Thr
|
|
ENST00000683557.1:c.*60G>A
|
ENSP00000508029.1:n.*60G>A
|
|
ENST00000367282.6:c.1228G>A
MANE Select
|
ENSP00000356251.4:p.Ala410Thr
|
|
ENST00000367282.5:c.1228G>A
|
ENSP00000356251.4:p.Ala410Thr
|
|
NM_004767.3:c.1228G>A
|
NP_004758.3:p.Ala410Thr
|
|
XM_011510158.1:c.667G>A
|
XP_011508460.1:p.Ala223Thr
|
|
NM_004767.4:c.1228G>A
|
NP_004758.3:p.Ala410Thr
|
|
XM_011510158.2:c.667G>A
|
XP_011508460.1:p.Ala223Thr
|
|
NM_004767.5:c.1228G>A
MANE Select
|
NP_004758.3:p.Ala410Thr
|
|