ENST00000559133.6:c.3589+259C>G
|
ENSP00000453958.2:n.3589+259C>G
|
|
ENST00000674301.2:c.3589+259C>G
|
ENSP00000501333.2:n.3589+259C>G
|
|
ENST00000684448.1:n.2263+259C>G
|
|
|
ENST00000316623.10:c.3589+259C>G
MANE Select
|
ENSP00000325527.5:n.3589+259C>G
|
|
ENST00000316623.9:c.3589+259C>G
|
ENSP00000325527.5:n.3589+259C>G
|
|
ENST00000537463.6:c.637-12166C>G
|
ENSP00000440294.2:n.637-12166C>G
|
|
NM_000138.4:c.3589+259C>G , LRG_778t1:c.3589+259C>G
|
NP_000129.3:n.3589+259C>G
|
|
NM_000138.5:c.3589+259C>G
MANE Select
|
NP_000129.3:n.3589+259C>G
|
|