ENST00000269321.12:c.416T>C
MANE Select
|
ENSP00000269321.7:p.Ile139Thr
|
|
ENST00000269321.11:c.416T>C
|
ENSP00000269321.7:p.Ile139Thr
|
|
ENST00000400721.8:c.415+98T>C
|
ENSP00000383556.4:n.415+98T>C
|
|
ENST00000541078.6:c.416T>C
|
ENSP00000441348.2:p.Ile139Thr
|
|
ENST00000578351.1:c.*60T>C
|
ENSP00000462323.1:n.*60T>C
|
|
ENST00000579121.5:c.416T>C
|
ENSP00000462960.1:p.Ile139Thr
|
|
ENST00000580033.5:c.*60T>C
|
ENSP00000463530.1:n.*60T>C
|
|
ENST00000580685.5:c.416T>C
|
ENSP00000464205.1:p.Ile139Thr
|
|
ENST00000581876.5:c.191T>C
|
ENSP00000461956.1:p.Val64Ala
|
|
ENST00000582984.5:n.618T>C
|
|
|
ENST00000583791.1:n.280T>C
|
|
|
ENST00000583868.5:c.416T>C
|
ENSP00000462209.1:p.Ile139Thr
|
|
ENST00000584461.5:c.416T>C
|
ENSP00000463939.1:p.Ile139Thr
|
|
NM_001185077.2:c.416T>C
|
NP_001172006.1:p.Ile139Thr
|
|
NM_001185078.2:c.415+98T>C
|
NP_001172007.1:n.415+98T>C
|
|
NM_001301240.1:c.416T>C
|
NP_001288169.1:p.Ile139Thr
|
|
NM_001301241.1:c.416T>C
|
NP_001288170.1:p.Ile139Thr
|
|
NM_001301242.1:c.416T>C
|
NP_001288171.1:p.Ile139Thr
|
|
NM_001301243.1:c.551T>C
|
NP_001288172.1:p.Ile184Thr
|
|
NM_004309.5:c.416T>C
|
NP_004300.1:p.Ile139Thr
|
|
NR_125441.1:n.475T>C
|
|
|
XM_011523574.1:c.551T>C
|
XP_011521876.1:p.Ile184Thr
|
|
NM_004309.6:c.416T>C
MANE Select
|
NP_004300.1:p.Ile139Thr
|
|
NM_001185077.3:c.416T>C
|
NP_001172006.1:p.Ile139Thr
|
|
NM_001185078.3:c.415+98T>C
|
NP_001172007.1:n.415+98T>C
|
|
NM_001301240.2:c.416T>C
|
NP_001288169.1:p.Ile139Thr
|
|
NM_001301241.2:c.416T>C
|
NP_001288170.1:p.Ile139Thr
|
|
NM_001301242.2:c.416T>C
|
NP_001288171.1:p.Ile139Thr
|
|
NM_001301243.2:c.551T>C
|
NP_001288172.1:p.Ile184Thr
|
|
NR_125441.2:n.406T>C
|
|
|