ENST00000471318.6:n.912T>C
|
|
|
ENST00000621467.5:c.990T>C
|
ENSP00000480508.2:p.Ser330=
|
|
ENST00000686475.1:n.1056T>C
|
|
|
ENST00000409883.7:c.1116T>C
MANE Select
|
ENSP00000386264.2:p.Ser372=
|
|
ENST00000286196.9:c.*680T>C
|
ENSP00000286196.5:n.*680T>C
|
|
ENST00000409444.6:c.1092T>C
|
ENSP00000387203.2:p.Ser364=
|
|
ENST00000409883.6:c.1116T>C
|
ENSP00000386264.2:p.Ser372=
|
|
ENST00000471318.5:n.344T>C
|
|
|
ENST00000495329.1:n.255T>C
|
|
|
ENST00000621467.4:c.1092T>C
|
ENSP00000480508.1:p.Ser364=
|
|
NM_001044385.2:c.1116T>C
|
NP_001037850.1:p.Ser372=
|
|
NM_152388.3:c.1092T>C
|
NP_689601.2:p.Ser364=
|
|
NM_001044385.3:c.1116T>C
MANE Select
|
NP_001037850.1:p.Ser372=
|
|
NM_152388.4:c.1092T>C
|
NP_689601.2:p.Ser364=
|
|