ENST00000426263.10:c.852G>T
MANE Select
|
ENSP00000416293.2:p.Leu284=
|
|
ENST00000674765.1:c.852G>T
|
ENSP00000501811.1:p.Leu284=
|
|
ENST00000675112.1:n.875G>T
|
|
|
ENST00000676254.1:n.1301G>T
|
|
|
ENST00000426263.7:c.852G>T
|
ENSP00000416293.2:p.Leu284=
|
|
ENST00000439722.2:c.731G>T
|
ENSP00000395521.2:n.731G>T
|
|
ENST00000475162.3:c.415+1018G>T
|
|
|
ENST00000630287.2:c.*167G>T
|
ENSP00000486694.1:n.*167G>T
|
|
NM_006516.2:c.852G>T
|
NP_006507.2:p.Leu284=
|
|
NM_006516.3:c.852G>T
|
NP_006507.2:p.Leu284=
|
|
NM_006516.4:c.852G>T
MANE Select
|
NP_006507.2:p.Leu284=
|
|