ENST00000682565.1:c.11733+98G>T
|
ENSP00000507671.1:n.11733+98G>T
|
|
ENST00000682801.1:c.11167-651G>T
|
ENSP00000507862.1:n.11167-651G>T
|
|
ENST00000682859.1:c.11733+98G>T
|
ENSP00000508222.1:n.11733+98G>T
|
|
ENST00000683791.1:c.4819+98G>T
|
|
|
ENST00000684460.1:c.9014+98G>T
|
|
|
ENST00000684548.1:c.11733+98G>T
|
ENSP00000507421.1:n.11733+98G>T
|
|
ENST00000684590.1:c.6180+98G>T
|
ENSP00000507376.1:n.6180+98G>T
|
|
ENST00000684656.1:c.9198+98G>T
|
|
|
ENST00000613296.6:c.12114+98G>T
MANE Select
|
ENSP00000482968.1:n.12114+98G>T
|
|
ENST00000651057.1:c.2268+98G>T
|
ENSP00000498504.1:n.2268+98G>T
|
|
ENST00000651434.1:c.3470+98G>T
|
|
|
ENST00000651750.1:c.1261-651G>T
|
|
|
ENST00000652487.1:c.3285+98G>T
|
|
|
ENST00000464408.3:n.289+98G>T
|
|
|
ENST00000484298.5:c.11988+98G>T
|
ENSP00000478155.1:n.11988+98G>T
|
|
ENST00000613296.4:c.12114+98G>T
|
ENSP00000482968.1:n.12114+98G>T
|
|
ENST00000620466.4:n.5917+98G>T
|
|
|
NM_015120.4:c.12117+98G>T , LRG_741t1:c.12117+98G>T
|
NP_055935.4:n.12117+98G>T
|
|
NM_001378454.1:c.12114+98G>T
MANE Select
|
NP_001365383.1:n.12114+98G>T
|
|