ENST00000682422.1:n.748G>A
|
|
|
ENST00000682545.1:c.*173G>A
|
ENSP00000508402.1:n.*173G>A
|
|
ENST00000682887.1:c.1568G>A
|
ENSP00000506946.1:n.1568G>A
|
|
ENST00000683302.1:c.1098G>A
|
ENSP00000507885.1:p.Leu366=
|
|
ENST00000683557.1:c.758G>A
|
ENSP00000508029.1:p.Ter253=
|
|
ENST00000367282.6:c.1167G>A
MANE Select
|
ENSP00000356251.4:p.Leu389=
|
|
ENST00000367282.5:c.1167G>A
|
ENSP00000356251.4:p.Leu389=
|
|
NM_004767.3:c.1167G>A
|
NP_004758.3:p.Leu389=
|
|
XM_011510158.1:c.606G>A
|
XP_011508460.1:p.Leu202=
|
|
NM_004767.4:c.1167G>A
|
NP_004758.3:p.Leu389=
|
|
XM_011510158.2:c.606G>A
|
XP_011508460.1:p.Leu202=
|
|
NM_004767.5:c.1167G>A
MANE Select
|
NP_004758.3:p.Leu389=
|
|