ENST00000348974.5:c.922G>T
|
ENSP00000330021.7:p.Gly308Trp
|
|
ENST00000394236.9:c.922G>T
MANE Select
|
ENSP00000377783.3:p.Gly308Trp
|
|
ENST00000407433.6:c.877G>T
|
ENSP00000385794.2:p.Gly293Trp
|
|
ENST00000647936.1:c.922G>T
|
ENSP00000496822.1:p.Gly308Trp
|
|
ENST00000648381.1:n.1090G>T
|
|
|
ENST00000648853.1:c.880G>T
|
ENSP00000497262.1:p.Gly294Trp
|
|
ENST00000649103.1:c.1021G>T
|
ENSP00000497962.1:n.1021G>T
|
|
ENST00000650591.1:c.1018G>T
|
ENSP00000497376.1:p.Gly340Trp
|
|
ENST00000394236.7:c.922G>T
|
ENSP00000377783.3:p.Gly308Trp
|
|
ENST00000407433.5:c.529G>T
|
ENSP00000385794.1:p.Gly177Trp
|
|
NM_000313.3:c.922G>T , LRG_572t1:c.922G>T
|
NP_000304.2:p.Gly308Trp
|
|
NM_001314077.1:c.1018G>T , LRG_572t2:c.1018G>T
|
NP_001301006.1:p.Gly340Trp
|
|
NM_000313.4:c.922G>T
MANE Select
|
NP_000304.2:p.Gly308Trp
|
|
NM_001314077.2:c.1018G>T
|
NP_001301006.1:p.Gly340Trp
|
|