ENST00000559133.6:c.4336+148G>T
|
ENSP00000453958.2:n.4336+148G>T
|
|
ENST00000674301.2:c.4336+148G>T
|
ENSP00000501333.2:n.4336+148G>T
|
|
ENST00000683268.1:n.303+148G>T
|
|
|
ENST00000684448.1:n.3010+148G>T
|
|
|
ENST00000316623.10:c.4336+148G>T
MANE Select
|
ENSP00000325527.5:n.4336+148G>T
|
|
ENST00000316623.9:c.4336+148G>T
|
ENSP00000325527.5:n.4336+148G>T
|
|
ENST00000537463.6:c.*99+148G>T
|
ENSP00000440294.2:n.*99+148G>T
|
|
NM_000138.4:c.4336+148G>T , LRG_778t1:c.4336+148G>T
|
NP_000129.3:n.4336+148G>T
|
|
NM_000138.5:c.4336+148G>T
MANE Select
|
NP_000129.3:n.4336+148G>T
|
|