ENST00000682565.1:c.10092A>G
|
ENSP00000507671.1:p.Pro3364=
|
|
ENST00000682801.1:c.10092A>G
|
ENSP00000507862.1:p.Pro3364=
|
|
ENST00000682859.1:c.10092A>G
|
ENSP00000508222.1:p.Pro3364=
|
|
ENST00000683791.1:c.3178A>G
|
|
|
ENST00000684460.1:c.7373A>G
|
|
|
ENST00000684548.1:c.10092A>G
|
ENSP00000507421.1:p.Pro3364=
|
|
ENST00000684590.1:c.4539A>G
|
ENSP00000507376.1:p.Pro1513=
|
|
ENST00000684656.1:c.7418A>G
|
|
|
ENST00000613296.6:c.10473A>G
MANE Select
|
ENSP00000482968.1:p.Pro3491=
|
|
ENST00000651057.1:c.627A>G
|
ENSP00000498504.1:p.Pro209=
|
|
ENST00000651434.1:c.1829A>G
|
|
|
ENST00000652487.1:c.1570A>G
|
|
|
ENST00000423048.5:c.3964A>G
|
ENSP00000399833.1:n.3964A>G
|
|
ENST00000484298.5:c.10347A>G
|
ENSP00000478155.1:p.Pro3449=
|
|
ENST00000613296.4:c.10473A>G
|
ENSP00000482968.1:p.Pro3491=
|
|
ENST00000614410.4:c.10473A>G
|
ENSP00000479094.1:p.Pro3491=
|
|
ENST00000620466.4:n.4276A>G
|
|
|
NM_015120.4:c.10476A>G , LRG_741t1:c.10476A>G
|
NP_055935.4:p.Pro3492=
|
|
NM_001378454.1:c.10473A>G
MANE Select
|
NP_001365383.1:p.Pro3491=
|
|