NM_001558.4:c.475A=
MANE Select
|
NP_001549.2:p.Ser159=
|
ENST00000227752.8:c.475A=
MANE Select
|
ENSP00000227752.4:p.Ser159=
|
NM_001558.3:c.475A= , LRG_151t1:c.475A=
|
NP_001549.2:p.Ser159=
|
NR_026691.1:n.682A=
|
|
NR_026691.2:n.679A=
|
|
ENST00000227752.7:c.475A=
|
ENSP00000227752.3:p.Ser159=
|
ENST00000525467.2:n.823A=
|
|
ENST00000526544.5:c.*11A=
|
ENSP00000435317.1:n.*11A=
|
ENST00000529924.5:n.2053A=
|
|
ENST00000529924.6:n.2053A=
|
|
ENST00000530178.1:n.341A=
|
|
ENST00000530761.5:n.852A=
|
|
ENST00000532009.1:n.291A=
|
|
ENST00000533700.5:n.682A=
|
|
ENST00000534335.1:n.295A=
|
|
ENST00000534574.5:c.*415A=
|
ENSP00000436328.1:n.*415A=
|
ENST00000696732.1:n.2324A=
|
|
XM_024448493.1:c.28A=
|
XP_024304261.1:p.Ser10=
|