|
NM_003762.5:c.404T>C
MANE Select
|
NP_003753.2:p.Ile135Thr
|
|
ENST00000236192.12:c.404T>C
MANE Select
|
ENSP00000236192.7:p.Ile135Thr
|
|
NM_001185127.1:c.401T>C
|
NP_001172056.1:p.Ile134Thr
|
|
NM_001185127.2:c.401T>C
|
NP_001172056.1:p.Ile134Thr
|
|
NM_003762.4:c.404T>C
|
NP_003753.2:p.Ile135Thr
|
|
NR_033704.1:n.783T>C
|
|
|
NR_033704.2:n.609T>C
|
|
|
ENST00000236192.11:c.404T>C
|
ENSP00000236192.7:p.Ile135Thr
|
|
ENST00000367740.2:c.401T>C
|
ENSP00000356714.2:p.Ile134Thr
|
|
ENST00000474047.5:c.404T>C
|
ENSP00000435933.1:p.Ile135Thr
|
|
ENST00000482519.1:n.563T>C
|
|
|
XM_017002713.2:c.*55T>C
|
XP_016858202.1:n.*55T>C
|
|
XR_426805.1:n.641T>C
|
|