ENST00000477151.2:n.303G>C
|
|
|
ENST00000643794.1:c.236G>C
|
ENSP00000495765.1:p.Arg79Thr
|
|
ENST00000651669.1:c.115G>C
MANE Select
|
ENSP00000499044.1:p.Gly39Arg
|
|
ENST00000368567.4:c.115G>C
|
ENSP00000357555.4:p.Gly39Arg
|
|
ENST00000392558.4:c.115G>C
|
ENSP00000376341.4:p.Gly39Arg
|
|
ENST00000477151.1:n.270G>C
|
|
|
ENST00000493224.5:n.381G>C
|
|
|
NM_001030.4:c.115G>C
|
NP_001021.1:p.Gly39Arg
|
|
NM_001030.6:c.115G>C
MANE Select
|
NP_001021.1:p.Gly39Arg
|
|
NM_001349946.1:c.19G>C
|
NP_001336875.1:p.Gly7Arg
|
|
NM_001349947.1:c.19G>C
|
NP_001336876.1:p.Gly7Arg
|
|
NM_001349946.2:c.19G>C
|
NP_001336875.1:p.Gly7Arg
|
|
NM_001349947.2:c.19G>C
|
NP_001336876.1:p.Gly7Arg
|
|