|
ENST00000337851.9:c.228T>C
MANE Select
|
ENSP00000338343.4:p.Gly76=
|
|
|
ENST00000337851.8:c.228T>C
|
ENSP00000338343.4:p.Gly76=
|
|
|
ENST00000435422.7:c.225T>C
|
ENSP00000403003.2:p.Gly75=
|
|
|
ENST00000517913.5:c.228T>C
|
ENSP00000429378.1:p.Gly76=
|
|
|
ENST00000524347.2:c.*92T>C
|
ENSP00000430794.1:n.*92T>C
|
|
|
NM_000337.5:c.228T>C , LRG_205t1:c.228T>C
|
NP_000328.2:p.Gly76=
|
|
|
NM_001128209.1:c.225T>C
|
NP_001121681.1:p.Gly75=
|
|
|
NM_172244.2:c.228T>C
|
NP_758447.1:p.Gly76=
|
|
|
XM_005265966.3:c.228T>C
|
XP_005266023.1:p.Gly76=
|
|
|
XM_005265967.1:c.228T>C
|
XP_005266024.1:p.Gly76=
|
|
|
XM_006714911.2:c.228T>C
|
XP_006714974.1:p.Gly76=
|
|
|
XM_011534621.1:c.225T>C
|
XP_011532923.1:p.Gly75=
|
|
|
XM_005265966.5:c.228T>C
|
XP_005266023.1:p.Gly76=
|
|
|
XM_005265967.2:c.228T>C
|
XP_005266024.1:p.Gly76=
|
|
|
XM_011534621.2:c.225T>C
|
XP_011532923.1:p.Gly75=
|
|
|
XM_017009723.2:c.228T>C
|
XP_016865212.1:p.Gly76=
|
|
|
XM_017009724.1:c.228T>C
|
XP_016865213.1:p.Gly76=
|
|
|
NM_001128209.2:c.225T>C
|
NP_001121681.1:p.Gly75=
|
|
|
NM_172244.3:c.228T>C
|
NP_758447.1:p.Gly76=
|
|
|
NM_000337.6:c.228T>C
MANE Select
|
NP_000328.2:p.Gly76=
|
|
