ENST00000355265.7:c.634G>C
MANE Select
|
ENSP00000347409.2:p.Gly212Arg
|
|
ENST00000467543.6:c.*486G>C
|
ENSP00000420011.2:n.*486G>C
|
|
ENST00000355265.6:c.634G>C
|
ENSP00000347409.2:p.Gly212Arg
|
|
ENST00000467543.5:c.577G>C
|
ENSP00000420011.1:p.Gly193Arg
|
|
ENST00000476829.5:c.525+439G>C
|
ENSP00000419889.1:n.525+439G>C
|
|
ENST00000479768.6:n.752G>C
|
|
|
ENST00000494148.1:n.233G>C
|
|
|
NM_000420.2:c.634G>C
|
NP_000411.1:p.Gly212Arg
|
|
XM_005249993.2:c.670G>C
|
XP_005250050.1:p.Gly224Arg
|
|
NM_000420.3:c.634G>C
MANE Select
|
NP_000411.1:p.Gly212Arg
|
|