ENST00000225927.7:c.383+129G>A
MANE Select
|
ENSP00000225927.1:n.383+129G>A
|
|
ENST00000225927.6:c.383+129G>A
|
ENSP00000225927.1:n.383+129G>A
|
|
ENST00000586516.5:c.133+129G>A
|
|
|
ENST00000591587.1:c.126+129G>A
|
ENSP00000467836.1:n.126+129G>A
|
|
NM_000263.3:c.383+129G>A
|
NP_000254.2:n.383+129G>A
|
|
XM_006721920.2:c.-360+129G>A
|
XP_006721983.1:n.-360+129G>A
|
|
XM_011524840.1:c.-360+129G>A
|
XP_011523142.1:n.-360+129G>A
|
|
XM_024450771.1:c.384-33G>A
|
XP_024306539.1:n.384-33G>A
|
|
NM_000263.4:c.383+129G>A
MANE Select
|
NP_000254.2:n.383+129G>A
|
|