ENST00000348974.5:c.908C=
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ENSP00000330021.7:p.Ala303=
|
|
ENST00000394236.9:c.908C=
MANE Select
|
ENSP00000377783.3:p.Ala303=
|
|
ENST00000407433.6:c.863C=
|
ENSP00000385794.2:p.Ala288=
|
|
ENST00000647936.1:c.908C=
|
ENSP00000496822.1:p.Ala303=
|
|
ENST00000648381.1:n.1076C=
|
|
|
ENST00000648853.1:c.866C=
|
ENSP00000497262.1:p.Ala289=
|
|
ENST00000649103.1:c.1007C=
|
ENSP00000497962.1:n.1007C=
|
|
ENST00000650591.1:c.1004C=
|
ENSP00000497376.1:p.Ala335=
|
|
ENST00000394236.7:c.908C=
|
ENSP00000377783.3:p.Ala303=
|
|
ENST00000407433.5:c.515C=
|
ENSP00000385794.1:p.Ala172=
|
|
NM_000313.3:c.908C= , LRG_572t1:c.908C=
|
NP_000304.2:p.Ala303=
|
|
NM_001314077.1:c.1004C= , LRG_572t2:c.1004C=
|
NP_001301006.1:p.Ala335=
|
|
NM_000313.4:c.908C=
MANE Select
|
NP_000304.2:p.Ala303=
|
|
NM_001314077.2:c.1004C=
|
NP_001301006.1:p.Ala335=
|
|