|
ENST00000367698.4:c.947T>C
MANE Select
|
ENSP00000356671.3:p.Ile316Thr
|
|
|
ENST00000367698.3:c.947T>C
|
ENSP00000356671.3:p.Ile316Thr
|
|
|
ENST00000487183.1:n.598T>C
|
|
|
|
ENST00000617423.4:c.559+2106T>C
|
ENSP00000478688.1:n.559+2106T>C
|
|
|
NM_000488.3:c.947T>C , LRG_577t1:c.947T>C
|
NP_000479.1:p.Ile316Thr
|
|
|
XM_005245198.2:c.803T>C
|
XP_005245255.1:p.Ile268Thr
|
|
|
NM_001365052.1:c.803T>C
|
NP_001351981.1:p.Ile268Thr
|
|
|
NM_000488.4:c.947T>C
MANE Select
|
NP_000479.1:p.Ile316Thr
|
|
|
NM_001365052.2:c.803T>C
|
NP_001351981.1:p.Ile268Thr
|
|
|
NM_001386302.1:c.1070T>C
|
NP_001373231.1:p.Ile357Thr
|
|
|
NM_001386303.1:c.1028T>C
|
NP_001373232.1:p.Ile343Thr
|
|
|
NM_001386304.1:c.926T>C
|
NP_001373233.1:p.Ile309Thr
|
|
|
NM_001386305.1:c.890T>C
|
NP_001373234.1:p.Ile297Thr
|
|
|
NM_001386306.1:c.731T>C
|
NP_001373235.1:p.Ile244Thr
|
|
