ENST00000487848.6:c.1175G>C
MANE Plus Clinical
|
ENSP00000417074.1:p.Gly392Ala
|
|
ENST00000696466.1:c.1457G>C
|
ENSP00000512647.1:p.Gly486Ala
|
|
ENST00000696672.1:c.150G>C
|
ENSP00000512796.1:p.Arg50Ser
|
|
ENST00000341105.7:c.1175G>C
MANE Select
|
ENSP00000345681.2:p.Gly392Ala
|
|
ENST00000341105.6:c.1175G>C
|
ENSP00000345681.2:p.Gly392Ala
|
|
ENST00000430265.6:c.1133G>C
|
ENSP00000400259.2:p.Gly378Ala
|
|
ENST00000487848.5:c.1175G>C
|
ENSP00000417074.1:p.Gly392Ala
|
|
ENST00000489987.1:n.292G>C
|
|
|
NM_001145661.1:c.1175G>C , LRG_295t1:c.1175G>C
|
NP_001139133.1:p.Gly392Ala
|
|
NM_001145662.1:c.1133G>C
|
NP_001139134.1:p.Gly378Ala
|
|
NM_032638.4:c.1175G>C , LRG_295t2:c.1175G>C
|
NP_116027.2:p.Gly392Ala
|
|
NM_001145661.2:c.1175G>C
MANE Plus Clinical
|
NP_001139133.1:p.Gly392Ala
|
|
NM_032638.5:c.1175G>C
MANE Select
|
NP_116027.2:p.Gly392Ala
|
|