ENST00000262367.10:c.4173T>A
MANE Select
|
ENSP00000262367.5:p.Tyr1391Ter
|
|
ENST00000262367.9:c.4173T>A
|
ENSP00000262367.5:p.Tyr1391Ter
|
|
ENST00000382070.7:c.4059T>A
|
ENSP00000371502.3:p.Tyr1353Ter
|
|
ENST00000570939.2:c.2808T>A
|
ENSP00000461002.2:p.Tyr936Ter
|
|
ENST00000573517.6:c.479T>A
|
|
|
ENST00000574740.1:n.215+714T>A
|
|
|
ENST00000576720.1:n.3110T>A
|
|
|
NM_001079846.1:c.4059T>A
|
NP_001073315.1:p.Tyr1353Ter
|
|
NM_004380.2:c.4173T>A
|
NP_004371.2:p.Tyr1391Ter
|
|
XM_005255124.3:c.4128T>A
|
XP_005255181.1:p.Tyr1376Ter
|
|
XM_005255125.3:c.3756T>A
|
XP_005255182.1:p.Tyr1252Ter
|
|
XM_006720848.2:c.4133+714T>A
|
XP_006720911.1:n.4133+714T>A
|
|
XM_011522380.1:c.4119T>A
|
XP_011520682.1:p.Tyr1373Ter
|
|
XM_011522381.1:c.3420T>A
|
XP_011520683.1:p.Tyr1140Ter
|
|
XM_005255124.4:c.4128T>A
|
XP_005255181.1:p.Tyr1376Ter
|
|
XM_005255125.4:c.3756T>A
|
XP_005255182.1:p.Tyr1252Ter
|
|
XM_006720848.3:c.4133+714T>A
|
XP_006720911.1:n.4133+714T>A
|
|
XM_011522381.2:c.3420T>A
|
XP_011520683.1:p.Tyr1140Ter
|
|
XM_017022944.1:c.4167T>A
|
XP_016878433.1:p.Tyr1389Ter
|
|
NM_004380.3:c.4173T>A
MANE Select
|
NP_004371.2:p.Tyr1391Ter
|
|