ENST00000487848.6:c.1321G>T
MANE Plus Clinical
|
ENSP00000417074.1:p.Gly441Cys
|
|
ENST00000696466.1:c.1603G>T
|
ENSP00000512647.1:p.Gly535Cys
|
|
ENST00000696672.1:c.296G>T
|
ENSP00000512796.1:p.Gly99Val
|
|
ENST00000341105.7:c.1321G>T
MANE Select
|
ENSP00000345681.2:p.Gly441Cys
|
|
ENST00000341105.6:c.1321G>T
|
ENSP00000345681.2:p.Gly441Cys
|
|
ENST00000430265.6:c.1279G>T
|
ENSP00000400259.2:p.Gly427Cys
|
|
ENST00000487848.5:c.1321G>T
|
ENSP00000417074.1:p.Gly441Cys
|
|
ENST00000489987.1:n.438G>T
|
|
|
NM_001145661.1:c.1321G>T , LRG_295t1:c.1321G>T
|
NP_001139133.1:p.Gly441Cys
|
|
NM_001145662.1:c.1279G>T
|
NP_001139134.1:p.Gly427Cys
|
|
NM_032638.4:c.1321G>T , LRG_295t2:c.1321G>T
|
NP_116027.2:p.Gly441Cys
|
|
NM_001145661.2:c.1321G>T
MANE Plus Clinical
|
NP_001139133.1:p.Gly441Cys
|
|
NM_032638.5:c.1321G>T
MANE Select
|
NP_116027.2:p.Gly441Cys
|
|