ENST00000617695.5:c.7733G>T
|
ENSP00000481744.2:p.Gly2578Val
|
|
ENST00000618192.5:c.8009G>T
|
ENSP00000480802.2:p.Gly2670Val
|
|
ENST00000421865.3:c.7745G>T
MANE Select
|
ENSP00000400365.2:p.Gly2582Val
|
|
ENST00000421865.2:c.7745G>T
|
ENSP00000400365.2:p.Gly2582Val
|
|
ENST00000617695.4:c.7733G>T
|
ENSP00000481744.1:p.Gly2578Val
|
|
ENST00000618192.4:c.7742G>T
|
ENSP00000480802.1:p.Gly2581Val
|
|
NM_000426.3:c.7745G>T , LRG_409t1:c.7745G>T
|
NP_000417.2:p.Gly2582Val
|
|
NM_001079823.1:c.7733G>T
|
NP_001073291.1:p.Gly2578Val
|
|
XM_005266981.2:c.8009G>T
|
XP_005267038.1:p.Gly2670Val
|
|
XM_005266982.2:c.7997G>T
|
XP_005267039.1:p.Gly2666Val
|
|
XM_011535820.1:c.8003G>T
|
XP_011534122.1:p.Gly2668Val
|
|
XM_005266981.3:c.8009G>T
|
XP_005267038.1:p.Gly2670Val
|
|
XM_005266982.3:c.7997G>T
|
XP_005267039.1:p.Gly2666Val
|
|
XM_011535820.2:c.8003G>T
|
XP_011534122.1:p.Gly2668Val
|
|
XM_017010851.2:c.8015G>T
|
XP_016866340.1:p.Gly2672Val
|
|
XM_017010852.1:c.6140G>T
|
XP_016866341.1:p.Gly2047Val
|
|
NM_000426.4:c.7745G>T
MANE Select
|
NP_000417.3:p.Gly2582Val
|
|
NM_001079823.2:c.7733G>T
|
NP_001073291.2:p.Gly2578Val
|
|