ENST00000262367.10:c.4171T>A
MANE Select
|
ENSP00000262367.5:p.Tyr1391Asn
|
|
ENST00000262367.9:c.4171T>A
|
ENSP00000262367.5:p.Tyr1391Asn
|
|
ENST00000382070.7:c.4057T>A
|
ENSP00000371502.3:p.Tyr1353Asn
|
|
ENST00000570939.2:c.2806T>A
|
ENSP00000461002.2:p.Tyr936Asn
|
|
ENST00000573517.6:c.477T>A
|
|
|
ENST00000574740.1:n.215+712T>A
|
|
|
ENST00000576720.1:n.3108T>A
|
|
|
NM_001079846.1:c.4057T>A
|
NP_001073315.1:p.Tyr1353Asn
|
|
NM_004380.2:c.4171T>A
|
NP_004371.2:p.Tyr1391Asn
|
|
XM_005255124.3:c.4126T>A
|
XP_005255181.1:p.Tyr1376Asn
|
|
XM_005255125.3:c.3754T>A
|
XP_005255182.1:p.Tyr1252Asn
|
|
XM_006720848.2:c.4133+712T>A
|
XP_006720911.1:n.4133+712T>A
|
|
XM_011522380.1:c.4117T>A
|
XP_011520682.1:p.Tyr1373Asn
|
|
XM_011522381.1:c.3418T>A
|
XP_011520683.1:p.Tyr1140Asn
|
|
XM_005255124.4:c.4126T>A
|
XP_005255181.1:p.Tyr1376Asn
|
|
XM_005255125.4:c.3754T>A
|
XP_005255182.1:p.Tyr1252Asn
|
|
XM_006720848.3:c.4133+712T>A
|
XP_006720911.1:n.4133+712T>A
|
|
XM_011522381.2:c.3418T>A
|
XP_011520683.1:p.Tyr1140Asn
|
|
XM_017022944.1:c.4165T>A
|
XP_016878433.1:p.Tyr1389Asn
|
|
NM_004380.3:c.4171T>A
MANE Select
|
NP_004371.2:p.Tyr1391Asn
|
|