ENST00000477151.2:n.286T>C
|
|
|
ENST00000643794.1:c.219T>C
|
ENSP00000495765.1:p.His73=
|
|
ENST00000651669.1:c.98T>C
MANE Select
|
ENSP00000499044.1:p.Met33Thr
|
|
ENST00000368567.4:c.98T>C
|
ENSP00000357555.4:p.Met33Thr
|
|
ENST00000392558.4:c.98T>C
|
ENSP00000376341.4:p.Met33Thr
|
|
ENST00000477151.1:n.253T>C
|
|
|
ENST00000493224.5:n.364T>C
|
|
|
NM_001030.4:c.98T>C
|
NP_001021.1:p.Met33Thr
|
|
NM_001030.6:c.98T>C
MANE Select
|
NP_001021.1:p.Met33Thr
|
|
NM_001349946.1:c.2T>C
|
NP_001336875.1:p.Met1Thr
|
|
NM_001349947.1:c.2T>C
|
NP_001336876.1:p.Met1Thr
|
|
NM_001349946.2:c.2T>C
|
NP_001336875.1:p.Met1Thr
|
|
NM_001349947.2:c.2T>C
|
NP_001336876.1:p.Met1Thr
|
|