ENST00000682565.1:c.10206T>G
|
ENSP00000507671.1:p.Pro3402=
|
|
ENST00000682801.1:c.10206T>G
|
ENSP00000507862.1:p.Pro3402=
|
|
ENST00000682859.1:c.10206T>G
|
ENSP00000508222.1:p.Pro3402=
|
|
ENST00000683791.1:c.3292T>G
|
|
|
ENST00000684460.1:c.7487T>G
|
|
|
ENST00000684548.1:c.10206T>G
|
ENSP00000507421.1:p.Pro3402=
|
|
ENST00000684590.1:c.4653T>G
|
ENSP00000507376.1:p.Pro1551=
|
|
ENST00000684656.1:c.7532T>G
|
|
|
ENST00000613296.6:c.10587T>G
MANE Select
|
ENSP00000482968.1:p.Pro3529=
|
|
ENST00000651057.1:c.741T>G
|
ENSP00000498504.1:p.Pro247=
|
|
ENST00000651434.1:c.1943T>G
|
|
|
ENST00000652487.1:c.1684T>G
|
|
|
ENST00000423048.5:c.4078T>G
|
ENSP00000399833.1:n.4078T>G
|
|
ENST00000484298.5:c.10461T>G
|
ENSP00000478155.1:p.Pro3487=
|
|
ENST00000613296.4:c.10587T>G
|
ENSP00000482968.1:p.Pro3529=
|
|
ENST00000614410.4:c.10587T>G
|
ENSP00000479094.1:p.Pro3529=
|
|
ENST00000620466.4:n.4390T>G
|
|
|
NM_015120.4:c.10590T>G , LRG_741t1:c.10590T>G
|
NP_055935.4:p.Pro3530=
|
|
NM_001378454.1:c.10587T>G
MANE Select
|
NP_001365383.1:p.Pro3529=
|
|