ENST00000258439.8:c.447G=
MANE Select
|
ENSP00000258439.3:p.Trp149=
|
|
ENST00000258439.7:c.447G=
|
ENSP00000258439.2:p.Trp149=
|
|
ENST00000432959.1:c.447G=
|
ENSP00000416660.1:p.Trp149=
|
|
ENST00000435268.1:c.195G=
|
ENSP00000411810.1:p.Trp65=
|
|
NM_001193304.2:c.447G=
|
NP_001180233.1:p.Trp149=
|
|
NM_017849.3:c.447G= , LRG_528t1:c.447G=
|
NP_060319.1:p.Trp149=
|
|
XM_017004450.1:c.-472G=
|
XP_016859939.1:n.-472G=
|
|
XM_017004452.1:c.195G=
|
XP_016859941.1:p.Trp65=
|
|
NM_001193304.3:c.447G=
|
NP_001180233.1:p.Trp149=
|
|
NM_017849.4:c.447G=
MANE Select
|
NP_060319.1:p.Trp149=
|
|