ENST00000435881.7:c.729T>C
MANE Select
|
ENSP00000416627.1:p.Leu243=
|
|
ENST00000246912.8:c.891T>C
|
ENSP00000246912.3:p.Leu297=
|
|
ENST00000346833.8:c.639T>C
|
ENSP00000320913.3:p.Leu213=
|
|
ENST00000435881.6:c.729T>C
|
ENSP00000416627.1:p.Leu243=
|
|
ENST00000585403.5:n.936T>C
|
|
|
ENST00000588320.1:n.1205T>C
|
|
|
ENST00000590050.5:n.895T>C
|
|
|
NM_170607.2:c.891T>C
|
NP_733752.1:p.Leu297=
|
|
NM_198204.1:c.729T>C
|
NP_937847.1:p.Leu243=
|
|
NM_198205.1:c.639T>C
|
NP_937848.1:p.Leu213=
|
|
NM_198204.2:c.729T>C
MANE Select
|
NP_937847.1:p.Leu243=
|
|
NM_170607.3:c.891T>C
|
NP_733752.1:p.Leu297=
|
|
NM_198205.2:c.639T>C
|
NP_937848.1:p.Leu213=
|
|