ENST00000426263.10:c.856G>C
MANE Select
|
ENSP00000416293.2:p.Gly286Arg
|
|
ENST00000674765.1:c.856G>C
|
ENSP00000501811.1:p.Gly286Arg
|
|
ENST00000675112.1:n.879G>C
|
|
|
ENST00000676254.1:n.1305G>C
|
|
|
ENST00000426263.7:c.856G>C
|
ENSP00000416293.2:p.Gly286Arg
|
|
ENST00000439722.2:c.735G>C
|
ENSP00000395521.2:n.735G>C
|
|
ENST00000475162.3:c.415+1022G>C
|
|
|
ENST00000630287.2:c.*171G>C
|
ENSP00000486694.1:n.*171G>C
|
|
NM_006516.2:c.856G>C
|
NP_006507.2:p.Gly286Arg
|
|
NM_006516.3:c.856G>C
|
NP_006507.2:p.Gly286Arg
|
|
NM_006516.4:c.856G>C
MANE Select
|
NP_006507.2:p.Gly286Arg
|
|