ENST00000682565.1:c.11712A>T
|
ENSP00000507671.1:p.Pro3904=
|
|
ENST00000682801.1:c.11167-770A>T
|
ENSP00000507862.1:n.11167-770A>T
|
|
ENST00000682859.1:c.11712A>T
|
ENSP00000508222.1:p.Pro3904=
|
|
ENST00000683791.1:c.4798A>T
|
|
|
ENST00000684460.1:c.8993A>T
|
|
|
ENST00000684548.1:c.11712A>T
|
ENSP00000507421.1:p.Pro3904=
|
|
ENST00000684590.1:c.6159A>T
|
ENSP00000507376.1:p.Pro2053=
|
|
ENST00000684656.1:c.9177A>T
|
|
|
ENST00000613296.6:c.12093A>T
MANE Select
|
ENSP00000482968.1:p.Pro4031=
|
|
ENST00000651057.1:c.2247A>T
|
ENSP00000498504.1:p.Pro749=
|
|
ENST00000651434.1:c.3449A>T
|
|
|
ENST00000651750.1:c.1260+534A>T
|
|
|
ENST00000652487.1:c.3264A>T
|
|
|
ENST00000464408.3:n.268A>T
|
|
|
ENST00000484298.5:c.11967A>T
|
ENSP00000478155.1:p.Pro3989=
|
|
ENST00000613296.4:c.12093A>T
|
ENSP00000482968.1:p.Pro4031=
|
|
ENST00000620466.4:n.5896A>T
|
|
|
NM_015120.4:c.12096A>T , LRG_741t1:c.12096A>T
|
NP_055935.4:p.Pro4032=
|
|
NM_001378454.1:c.12093A>T
MANE Select
|
NP_001365383.1:p.Pro4031=
|
|