ENST00000477151.2:n.235A>C
|
|
|
ENST00000643794.1:c.168A>C
|
ENSP00000495765.1:p.Glu56Asp
|
|
ENST00000651669.1:c.47A>C
MANE Select
|
ENSP00000499044.1:p.Lys16Thr
|
|
ENST00000368567.4:c.47A>C
|
ENSP00000357555.4:p.Lys16Thr
|
|
ENST00000392558.4:c.47A>C
|
ENSP00000376341.4:p.Lys16Thr
|
|
ENST00000477151.1:n.202A>C
|
|
|
ENST00000493224.5:n.313A>C
|
|
|
NM_001030.4:c.47A>C
|
NP_001021.1:p.Lys16Thr
|
|
NM_001030.6:c.47A>C
MANE Select
|
NP_001021.1:p.Lys16Thr
|
|
NM_001349946.1:c.-50A>C
|
NP_001336875.1:n.-50A>C
|
|
NM_001349947.1:c.-50A>C
|
NP_001336876.1:n.-50A>C
|
|
NM_001349946.2:c.-50A>C
|
NP_001336875.1:n.-50A>C
|
|
NM_001349947.2:c.-50A>C
|
NP_001336876.1:n.-50A>C
|
|