ENST00000682565.1:c.11677C>A
|
ENSP00000507671.1:p.Pro3893Thr
|
|
ENST00000682801.1:c.11167-805C>A
|
ENSP00000507862.1:n.11167-805C>A
|
|
ENST00000682859.1:c.11677C>A
|
ENSP00000508222.1:p.Pro3893Thr
|
|
ENST00000683791.1:c.4763C>A
|
|
|
ENST00000684460.1:c.8958C>A
|
|
|
ENST00000684548.1:c.11677C>A
|
ENSP00000507421.1:p.Pro3893Thr
|
|
ENST00000684590.1:c.6124C>A
|
ENSP00000507376.1:p.Pro2042Thr
|
|
ENST00000684656.1:c.9142C>A
|
|
|
ENST00000613296.6:c.12058C>A
MANE Select
|
ENSP00000482968.1:p.Pro4020Thr
|
|
ENST00000651057.1:c.2212C>A
|
ENSP00000498504.1:p.Pro738Thr
|
|
ENST00000651434.1:c.3414C>A
|
|
|
ENST00000651750.1:c.1260+499C>A
|
|
|
ENST00000652487.1:c.3229C>A
|
|
|
ENST00000464408.3:n.233C>A
|
|
|
ENST00000484298.5:c.11932C>A
|
ENSP00000478155.1:p.Pro3978Thr
|
|
ENST00000613296.4:c.12058C>A
|
ENSP00000482968.1:p.Pro4020Thr
|
|
ENST00000620466.4:n.5861C>A
|
|
|
NM_015120.4:c.12061C>A , LRG_741t1:c.12061C>A
|
NP_055935.4:p.Pro4021Thr
|
|
NM_001378454.1:c.12058C>A
MANE Select
|
NP_001365383.1:p.Pro4020Thr
|
|