ENST00000696142.1:c.*313A>C
|
ENSP00000512434.1:n.*313A>C
|
|
ENST00000696143.1:c.772A>C
|
ENSP00000512435.1:n.772A>C
|
|
ENST00000696153.1:c.747A>C
|
ENSP00000512444.1:p.Gly249=
|
|
ENST00000256474.3:c.636A>C
MANE Select
|
ENSP00000256474.3:p.Gly212=
|
|
ENST00000256474.2:c.636A>C
|
ENSP00000256474.2:p.Gly212=
|
|
ENST00000345392.2:c.513A>C
|
ENSP00000344757.2:p.Gly171=
|
|
ENST00000477538.1:n.772A>C
|
|
|
NM_000551.3:c.636A>C , LRG_322t1:c.636A>C
|
NP_000542.1:p.Gly212=
|
|
NM_198156.2:c.513A>C
|
NP_937799.1:p.Gly171=
|
|
NM_001354723.1:c.*190A>C
|
NP_001341652.1:n.*190A>C
|
|
NM_000551.4:c.636A>C
MANE Select
|
NP_000542.1:p.Gly212=
|
|
NM_001354723.2:c.*190A>C
|
NP_001341652.1:n.*190A>C
|
|
NM_198156.3:c.513A>C
|
NP_937799.1:p.Gly171=
|
|