ENST00000547400.6:c.355+422T>G
|
ENSP00000446724.2:n.355+422T>G
|
|
ENST00000551576.6:c.525+2T>G
|
ENSP00000455848.2:n.525+2T>G
|
|
ENST00000552678.2:c.525+2T>G
|
ENSP00000457394.2:n.525+2T>G
|
|
ENST00000388922.9:c.525+2T>G
MANE Select
|
ENSP00000373574.4:n.525+2T>G
|
|
ENST00000388922.8:c.525+2T>G
|
ENSP00000373574.4:n.525+2T>G
|
|
ENST00000419526.6:c.104-667T>G
|
ENSP00000392492.2:n.104-667T>G
|
|
ENST00000547400.5:c.355+422T>G
|
ENSP00000446724.1:n.355+422T>G
|
|
ENST00000550683.5:c.567+2T>G
|
ENSP00000447884.1:n.567+2T>G
|
|
NM_000020.2:c.525+2T>G , LRG_543t1:c.525+2T>G
|
NP_000011.2:n.525+2T>G
|
|
NM_001077401.1:c.525+2T>G
|
NP_001070869.1:n.525+2T>G
|
|
XM_005269235.2:c.525+2T>G
|
XP_005269292.1:n.525+2T>G
|
|
XM_011539008.1:c.355+422T>G
|
XP_011537310.1:n.355+422T>G
|
|
XM_024449279.1:c.-165+2T>G
|
XP_024305047.1:n.-165+2T>G
|
|
NM_000020.3:c.525+2T>G
MANE Select
|
NP_000011.2:n.525+2T>G
|
|
NM_001077401.2:c.525+2T>G
|
NP_001070869.1:n.525+2T>G
|
|