ENST00000682565.1:c.10565G>C
|
ENSP00000507671.1:p.Ser3522Thr
|
|
ENST00000682801.1:c.10565G>C
|
ENSP00000507862.1:p.Ser3522Thr
|
|
ENST00000682859.1:c.10565G>C
|
ENSP00000508222.1:p.Ser3522Thr
|
|
ENST00000683791.1:c.3651G>C
|
|
|
ENST00000684460.1:c.7846G>C
|
|
|
ENST00000684548.1:c.10565G>C
|
ENSP00000507421.1:p.Ser3522Thr
|
|
ENST00000684590.1:c.5012G>C
|
ENSP00000507376.1:p.Ser1671Thr
|
|
ENST00000684656.1:c.7891G>C
|
|
|
ENST00000613296.6:c.10946G>C
MANE Select
|
ENSP00000482968.1:p.Ser3649Thr
|
|
ENST00000651057.1:c.1100G>C
|
ENSP00000498504.1:p.Ser367Thr
|
|
ENST00000651434.1:c.2302G>C
|
|
|
ENST00000651750.1:c.334G>C
|
|
|
ENST00000652487.1:c.2043G>C
|
|
|
ENST00000423048.5:c.4437G>C
|
ENSP00000399833.1:n.4437G>C
|
|
ENST00000484298.5:c.10820G>C
|
ENSP00000478155.1:p.Ser3607Thr
|
|
ENST00000613296.4:c.10946G>C
|
ENSP00000482968.1:p.Ser3649Thr
|
|
ENST00000614410.4:c.10946G>C
|
ENSP00000479094.1:p.Ser3649Thr
|
|
ENST00000620466.4:n.4749G>C
|
|
|
NM_015120.4:c.10949G>C , LRG_741t1:c.10949G>C
|
NP_055935.4:p.Ser3650Thr
|
|
NM_001378454.1:c.10946G>C
MANE Select
|
NP_001365383.1:p.Ser3649Thr
|
|