ENST00000682565.1:c.10580G>C
|
ENSP00000507671.1:p.Ser3527Thr
|
|
ENST00000682801.1:c.10580G>C
|
ENSP00000507862.1:p.Ser3527Thr
|
|
ENST00000682859.1:c.10580G>C
|
ENSP00000508222.1:p.Ser3527Thr
|
|
ENST00000683791.1:c.3666G>C
|
|
|
ENST00000684460.1:c.7861G>C
|
|
|
ENST00000684548.1:c.10580G>C
|
ENSP00000507421.1:p.Ser3527Thr
|
|
ENST00000684590.1:c.5027G>C
|
ENSP00000507376.1:p.Ser1676Thr
|
|
ENST00000684656.1:c.7906G>C
|
|
|
ENST00000613296.6:c.10961G>C
MANE Select
|
ENSP00000482968.1:p.Ser3654Thr
|
|
ENST00000651057.1:c.1115G>C
|
ENSP00000498504.1:p.Ser372Thr
|
|
ENST00000651434.1:c.2317G>C
|
|
|
ENST00000651750.1:c.349G>C
|
|
|
ENST00000652487.1:c.2058G>C
|
|
|
ENST00000423048.5:c.4452G>C
|
ENSP00000399833.1:n.4452G>C
|
|
ENST00000484298.5:c.10835G>C
|
ENSP00000478155.1:p.Ser3612Thr
|
|
ENST00000613296.4:c.10961G>C
|
ENSP00000482968.1:p.Ser3654Thr
|
|
ENST00000614410.4:c.10961G>C
|
ENSP00000479094.1:p.Ser3654Thr
|
|
ENST00000620466.4:n.4764G>C
|
|
|
NM_015120.4:c.10964G>C , LRG_741t1:c.10964G>C
|
NP_055935.4:p.Ser3655Thr
|
|
NM_001378454.1:c.10961G>C
MANE Select
|
NP_001365383.1:p.Ser3654Thr
|
|