ENST00000330062.8:c.401G>C
MANE Select
|
ENSP00000331897.4:p.Ser134Thr
|
|
ENST00000330062.7:c.401G>C
|
ENSP00000331897.3:p.Ser134Thr
|
|
ENST00000540499.2:c.245G>C
|
ENSP00000446147.2:p.Ser82Thr
|
|
ENST00000559482.5:c.208-218G>C
|
ENSP00000453016.1:n.208-218G>C
|
|
ENST00000560061.1:c.*26G>C
|
ENSP00000453254.1:n.*26G>C
|
|
NM_001289910.1:c.245G>C , LRG_611t1:c.245G>C
|
NP_001276839.1:p.Ser82Thr
|
|
NM_001290114.1:c.11G>C
|
NP_001277043.1:p.Ser4Thr
|
|
NM_002168.3:c.401G>C , LRG_611t2:c.401G>C
|
NP_002159.2:p.Ser134Thr
|
|
NM_001290114.2:c.11G>C
|
NP_001277043.1:p.Ser4Thr
|
|
NM_002168.4:c.401G>C
MANE Select
|
NP_002159.2:p.Ser134Thr
|
|