ENST00000262367.10:c.4399G>T
MANE Select
|
ENSP00000262367.5:p.Val1467Leu
|
|
ENST00000262367.9:c.4399G>T
|
ENSP00000262367.5:p.Val1467Leu
|
|
ENST00000382070.7:c.4285G>T
|
ENSP00000371502.3:p.Val1429Leu
|
|
ENST00000570939.2:c.3034G>T
|
ENSP00000461002.2:p.Val1012Leu
|
|
ENST00000571763.5:n.189G>T
|
|
|
ENST00000574740.1:n.220G>T
|
|
|
ENST00000576720.1:n.3222G>T
|
|
|
NM_001079846.1:c.4285G>T
|
NP_001073315.1:p.Val1429Leu
|
|
NM_004380.2:c.4399G>T
|
NP_004371.2:p.Val1467Leu
|
|
XM_005255124.3:c.4354G>T
|
XP_005255181.1:p.Val1452Leu
|
|
XM_005255125.3:c.3982G>T
|
XP_005255182.1:p.Val1328Leu
|
|
XM_006720848.2:c.4138G>T
|
XP_006720911.1:p.Val1380Leu
|
|
XM_011522380.1:c.4345G>T
|
XP_011520682.1:p.Val1449Leu
|
|
XM_011522381.1:c.3646G>T
|
XP_011520683.1:p.Val1216Leu
|
|
XM_005255124.4:c.4354G>T
|
XP_005255181.1:p.Val1452Leu
|
|
XM_005255125.4:c.3982G>T
|
XP_005255182.1:p.Val1328Leu
|
|
XM_006720848.3:c.4138G>T
|
XP_006720911.1:p.Val1380Leu
|
|
XM_011522381.2:c.3646G>T
|
XP_011520683.1:p.Val1216Leu
|
|
XM_017022944.1:c.4393G>T
|
XP_016878433.1:p.Val1465Leu
|
|
NM_004380.3:c.4399G>T
MANE Select
|
NP_004371.2:p.Val1467Leu
|
|