ENST00000617695.5:c.6912A>G
|
ENSP00000481744.2:p.Gly2304=
|
|
ENST00000618192.5:c.7176A>G
|
ENSP00000480802.2:p.Gly2392=
|
|
ENST00000684985.1:n.543A>G
|
|
|
ENST00000688150.1:n.251A>G
|
|
|
ENST00000421865.3:c.6912A>G
MANE Select
|
ENSP00000400365.2:p.Gly2304=
|
|
ENST00000421865.2:c.6912A>G
|
ENSP00000400365.2:p.Gly2304=
|
|
ENST00000617695.4:c.6912A>G
|
ENSP00000481744.1:p.Gly2304=
|
|
ENST00000618192.4:c.6909A>G
|
ENSP00000480802.1:p.Gly2303=
|
|
NM_000426.3:c.6912A>G , LRG_409t1:c.6912A>G
|
NP_000417.2:p.Gly2304=
|
|
NM_001079823.1:c.6912A>G
|
NP_001073291.1:p.Gly2304=
|
|
XM_005266981.2:c.7176A>G
|
XP_005267038.1:p.Gly2392=
|
|
XM_005266982.2:c.7176A>G
|
XP_005267039.1:p.Gly2392=
|
|
XM_011535820.1:c.7170A>G
|
XP_011534122.1:p.Gly2390=
|
|
XM_005266981.3:c.7176A>G
|
XP_005267038.1:p.Gly2392=
|
|
XM_005266982.3:c.7176A>G
|
XP_005267039.1:p.Gly2392=
|
|
XM_011535820.2:c.7170A>G
|
XP_011534122.1:p.Gly2390=
|
|
XM_017010851.2:c.7182A>G
|
XP_016866340.1:p.Gly2394=
|
|
XM_017010852.1:c.5307A>G
|
XP_016866341.1:p.Gly1769=
|
|
NM_000426.4:c.6912A>G
MANE Select
|
NP_000417.3:p.Gly2304=
|
|
NM_001079823.2:c.6912A>G
|
NP_001073291.2:p.Gly2304=
|
|