ENST00000426263.10:c.405G>T
MANE Select
|
ENSP00000416293.2:p.Leu135=
|
|
ENST00000674765.1:c.405G>T
|
ENSP00000501811.1:p.Leu135=
|
|
ENST00000675112.1:n.428G>T
|
|
|
ENST00000676254.1:n.854G>T
|
|
|
ENST00000372500.4:c.309G>T
|
ENSP00000361578.4:p.Leu103=
|
|
ENST00000426263.7:c.405G>T
|
ENSP00000416293.2:p.Leu135=
|
|
ENST00000439722.2:c.284G>T
|
ENSP00000395521.2:n.284G>T
|
|
ENST00000475162.3:c.304G>T
|
|
|
ENST00000625233.2:n.613G>T
|
|
|
ENST00000630287.2:c.405G>T
|
ENSP00000486694.1:p.Leu135=
|
|
NM_006516.2:c.405G>T
|
NP_006507.2:p.Leu135=
|
|
NM_006516.3:c.405G>T
|
NP_006507.2:p.Leu135=
|
|
NM_006516.4:c.405G>T
MANE Select
|
NP_006507.2:p.Leu135=
|
|