ENST00000262367.10:c.4556A>T
MANE Select
|
ENSP00000262367.5:p.Tyr1519Phe
|
|
ENST00000262367.9:c.4556A>T
|
ENSP00000262367.5:p.Tyr1519Phe
|
|
ENST00000382070.7:c.4442A>T
|
ENSP00000371502.3:p.Tyr1481Phe
|
|
ENST00000570939.2:c.3191A>T
|
ENSP00000461002.2:p.Tyr1064Phe
|
|
ENST00000571763.5:n.346A>T
|
|
|
ENST00000574740.1:n.377A>T
|
|
|
ENST00000576720.1:n.3379A>T
|
|
|
NM_001079846.1:c.4442A>T
|
NP_001073315.1:p.Tyr1481Phe
|
|
NM_004380.2:c.4556A>T
|
NP_004371.2:p.Tyr1519Phe
|
|
XM_005255124.3:c.4511A>T
|
XP_005255181.1:p.Tyr1504Phe
|
|
XM_005255125.3:c.4139A>T
|
XP_005255182.1:p.Tyr1380Phe
|
|
XM_006720848.2:c.4295A>T
|
XP_006720911.1:p.Tyr1432Phe
|
|
XM_011522380.1:c.4502A>T
|
XP_011520682.1:p.Tyr1501Phe
|
|
XM_011522381.1:c.3803A>T
|
XP_011520683.1:p.Tyr1268Phe
|
|
XM_005255124.4:c.4511A>T
|
XP_005255181.1:p.Tyr1504Phe
|
|
XM_005255125.4:c.4139A>T
|
XP_005255182.1:p.Tyr1380Phe
|
|
XM_006720848.3:c.4295A>T
|
XP_006720911.1:p.Tyr1432Phe
|
|
XM_011522381.2:c.3803A>T
|
XP_011520683.1:p.Tyr1268Phe
|
|
XM_017022944.1:c.4550A>T
|
XP_016878433.1:p.Tyr1517Phe
|
|
NM_004380.3:c.4556A>T
MANE Select
|
NP_004371.2:p.Tyr1519Phe
|
|