ENST00000682422.1:n.757G>C
|
|
|
ENST00000682545.1:c.*182G>C
|
ENSP00000508402.1:n.*182G>C
|
|
ENST00000682887.1:c.1577G>C
|
ENSP00000506946.1:n.1577G>C
|
|
ENST00000683302.1:c.1107G>C
|
ENSP00000507885.1:p.Gln369His
|
|
ENST00000683557.1:c.*8G>C
|
ENSP00000508029.1:n.*8G>C
|
|
ENST00000367282.6:c.1176G>C
MANE Select
|
ENSP00000356251.4:p.Gln392His
|
|
ENST00000367282.5:c.1176G>C
|
ENSP00000356251.4:p.Gln392His
|
|
NM_004767.3:c.1176G>C
|
NP_004758.3:p.Gln392His
|
|
XM_011510158.1:c.615G>C
|
XP_011508460.1:p.Gln205His
|
|
NM_004767.4:c.1176G>C
|
NP_004758.3:p.Gln392His
|
|
XM_011510158.2:c.615G>C
|
XP_011508460.1:p.Gln205His
|
|
NM_004767.5:c.1176G>C
MANE Select
|
NP_004758.3:p.Gln392His
|
|