ENST00000682422.1:n.852G>T
|
|
|
ENST00000682545.1:c.*277G>T
|
ENSP00000508402.1:n.*277G>T
|
|
ENST00000682887.1:c.1672G>T
|
ENSP00000506946.1:n.1672G>T
|
|
ENST00000683302.1:c.1202G>T
|
ENSP00000507885.1:p.Gly401Val
|
|
ENST00000683557.1:c.*103G>T
|
ENSP00000508029.1:n.*103G>T
|
|
ENST00000367282.6:c.1271G>T
MANE Select
|
ENSP00000356251.4:p.Gly424Val
|
|
ENST00000367282.5:c.1271G>T
|
ENSP00000356251.4:p.Gly424Val
|
|
NM_004767.3:c.1271G>T
|
NP_004758.3:p.Gly424Val
|
|
XM_011510158.1:c.710G>T
|
XP_011508460.1:p.Gly237Val
|
|
NM_004767.4:c.1271G>T
|
NP_004758.3:p.Gly424Val
|
|
XM_011510158.2:c.710G>T
|
XP_011508460.1:p.Gly237Val
|
|
NM_004767.5:c.1271G>T
MANE Select
|
NP_004758.3:p.Gly424Val
|
|