ENST00000682565.1:c.11679A>G
|
ENSP00000507671.1:p.Pro3893=
|
|
ENST00000682801.1:c.11167-803A>G
|
ENSP00000507862.1:n.11167-803A>G
|
|
ENST00000682859.1:c.11679A>G
|
ENSP00000508222.1:p.Pro3893=
|
|
ENST00000683791.1:c.4765A>G
|
|
|
ENST00000684460.1:c.8960A>G
|
|
|
ENST00000684548.1:c.11679A>G
|
ENSP00000507421.1:p.Pro3893=
|
|
ENST00000684590.1:c.6126A>G
|
ENSP00000507376.1:p.Pro2042=
|
|
ENST00000684656.1:c.9144A>G
|
|
|
ENST00000613296.6:c.12060A>G
MANE Select
|
ENSP00000482968.1:p.Pro4020=
|
|
ENST00000651057.1:c.2214A>G
|
ENSP00000498504.1:p.Pro738=
|
|
ENST00000651434.1:c.3416A>G
|
|
|
ENST00000651750.1:c.1260+501A>G
|
|
|
ENST00000652487.1:c.3231A>G
|
|
|
ENST00000464408.3:n.235A>G
|
|
|
ENST00000484298.5:c.11934A>G
|
ENSP00000478155.1:p.Pro3978=
|
|
ENST00000613296.4:c.12060A>G
|
ENSP00000482968.1:p.Pro4020=
|
|
ENST00000620466.4:n.5863A>G
|
|
|
NM_015120.4:c.12063A>G , LRG_741t1:c.12063A>G
|
NP_055935.4:p.Pro4021=
|
|
NM_001378454.1:c.12060A>G
MANE Select
|
NP_001365383.1:p.Pro4020=
|
|