ENST00000426263.10:c.693G>T
MANE Select
|
ENSP00000416293.2:p.Leu231=
|
|
ENST00000669445.1:c.57-34G>T
|
|
|
ENST00000674765.1:c.693G>T
|
ENSP00000501811.1:p.Leu231=
|
|
ENST00000675112.1:n.716G>T
|
|
|
ENST00000676254.1:n.1142G>T
|
|
|
ENST00000426263.7:c.693G>T
|
ENSP00000416293.2:p.Leu231=
|
|
ENST00000439722.2:c.572G>T
|
ENSP00000395521.2:n.572G>T
|
|
ENST00000475162.3:c.415+859G>T
|
|
|
ENST00000630287.2:c.*8G>T
|
ENSP00000486694.1:n.*8G>T
|
|
NM_006516.2:c.693G>T
|
NP_006507.2:p.Leu231=
|
|
NM_006516.3:c.693G>T
|
NP_006507.2:p.Leu231=
|
|
NM_006516.4:c.693G>T
MANE Select
|
NP_006507.2:p.Leu231=
|
|