ENST00000200676.8:c.1249-157G>A
MANE Select
|
ENSP00000200676.3:n.1249-157G>A
|
|
ENST00000650358.1:n.1647-157G>A
|
|
|
ENST00000200676.7:c.1249-157G>A
|
ENSP00000200676.3:n.1249-157G>A
|
|
ENST00000379780.6:c.1069-157G>A
|
ENSP00000369106.2:n.1069-157G>A
|
|
ENST00000566128.1:c.1054-157G>A
|
ENSP00000456276.1:n.1054-157G>A
|
|
NM_000078.2:c.1249-157G>A
|
NP_000069.2:n.1249-157G>A
|
|
NM_001286085.1:c.1069-157G>A
|
NP_001273014.1:n.1069-157G>A
|
|
NM_000078.3:c.1249-157G>A
MANE Select
|
NP_000069.2:n.1249-157G>A
|
|
NM_001286085.2:c.1069-157G>A
|
NP_001273014.1:n.1069-157G>A
|
|